Stem Cell Therapy for Erectile Dysfunction (ED)
Erectile dysfunction (ED) is defined as persistent difficulty achieving or maintaining an erection sufficient for satisfactory sexual activity. It affects approximately 50% of men between the ages of 40 and 70.
Approximately 80% of ED cases have an identifiable physical cause, while around 10% are primarily associated with psychological factors. Conventional treatments can help manage ED, but they do not always restore natural erectile function.
At ANOVA IRM in Offenbach, Germany, selected patients may be evaluated for an autologous stem cell-based treatment approach. The treatment concept primarily focuses on Mesenchymal Stem Cell Secretome / Exosome therapy, also known as MSEC therapy, and is considered alongside established treatment options.
This page provides an overview of ED causes, established treatment options, precision diagnostics and ANOVA's stem cell-based approach. Stem cell-based treatment for ED remains experimental and requires an individual medical review to determine whether it is appropriate.
Erectile Dysfunction Treatment Overview
Jump directly to the following topics:
- Stem cell therapy for erectile dysfunction at ANOVA IRM
- Can stem cell therapy help erectile dysfunction?
- ANOVA IRM’s treatment approach for ED
- Expected outcomes and treatment limitations
- Potency hypothesis of stem cell therapies
- MSEC / Stem Cell Secretome / Exosome-containing therapy
- Candidate suitability and exclusion criteria
- Treatment workflow, timeline and travel requirements
- Cost and insurance coverage
- Medical evaluation and FAQs

MSC secretome - exosome - therapy
ANOVA IRM - Germany
Stem Cell Therapy for Erectile Dysfunction at ANOVA IRM
Stem cell-based therapy may be considered alongside appropriate established ED treatment rather than as a replacement.
Conventional treatment options for ED include:
- Improving penile blood flow with oral PDE5 inhibitors such as sildenafil or tadalafil
- Addressing cardiovascular, metabolic, hormonal, medication-related or lifestyle contributors
- Providing psychological or psychosexual support when relevant
- Supporting erections through injectable or intraurethral medication, vacuum devices or a penile prosthesis
PDE5 inhibitors are often used as first-line treatment and help many patients. However, some cannot take or tolerate them, while others do not achieve the desired response. Other options vary in invasiveness and may not suit every patient.
Even with treatment, spontaneous erectile function may remain impaired when underlying vascular changes, cavernosal nerve injury, or tissue damage persist.
This has encouraged research into regenerative approaches that examine the biological environment involved in erectile function. At ANOVA IRM, selected patients may be assessed for autologous MSEC therapy alongside appropriate established care.
Can Stem Cell Therapy Help Erectile Dysfunction?
Stem cell-based therapy for ED is being investigated as a regenerative approach, particularly when vascular, nerve or erectile-tissue damage contributes to symptoms.
Why Physical ED Is Relevant to Regenerative Research
Physical, or organic, ED can develop when blood flow, nerve signalling or smooth-muscle relaxation within the penis is impaired. Difficulty restricting venous outflow may also prevent an erection from being maintained.
Cavernous nerve injury following radical prostatectomy and conditions such as diabetes can disrupt these processes. Over time, ongoing damage may contribute to endothelial dysfunction, smooth-muscle loss and fibrosis within the erectile tissue.
Researchers have therefore studied how stem cells and stem cell-derived products may influence:
- Blood-vessel signalling and the function of endothelial cells
- Cavernous nerve injury and nerve-support pathways
- Smooth muscle cell survival and function
- Inflammation, oxidative stress and metabolic injury
- Fibrosis and other tissue-remodelling processes
Most evidence for these proposed mechanisms is preclinical, meaning it comes from laboratory and animal studies. Human research remains limited to small phase I and II trials that used different living-cell products, treatment methods and patient groups. Some studies reported improvements, but the findings have varied and current evidence remains insufficient to support a clinical recommendation.
Because these studies evaluated living-cell products rather than ANOVA's cell-free MSEC therapy, they provide scientific background for the broader regenerative rationale rather than direct evidence for MSEC. MSEC contains no living stem cells; its rationale concerns the biological signals released by mesenchymal stem cells.
Whether that rationale may be relevant to an individual patient depends partly on the physical processes contributing to their ED. Identifying those processes is therefore an important part of ANOVA's assessment.
ED Diagnostics at ANOVA IRM: Revealing the Cause and Severity
Because ED often has more than one contributing factor, a comprehensive diagnostic assessment may be needed before an appropriate treatment approach can be determined.
ANOVA conducts advanced imaging in cooperation with the Prof. Stehling Institute for Diagnostic Imaging, located in the same building, drawing on Dr. Michael K. Stehling's background in radiology and physics.
Depending on the individual case, ANOVA's diagnostic assessment may include:
- An ED questionnaire assessing general health, sexual function and specific symptoms
- A physical examination by a urologist or andrologist
- Blood testing, which may include glucose or HbA1c, a lipid profile and relevant hormone values such as testosterone
- Doppler or duplex ultrasound of the penis and penile arteries
- SKAT-MRI, a penile MRI performed during a pharmacologically induced erection, to evaluate structural and vascular contributors in selected cases
The results help identify underlying conditions that may require established treatment and inform whether MSEC therapy may be medically appropriate.

The erectile system of the penis. “Cross-Sectional Anatomy of the Penis” by Philschatz. License: CC BY 4.0. ANOVA IRM - Germany

Erectile dysfunction - diagnostics:
A 43-year-old patient: (a) pharmacocavernosography does not show venous leakage clearly. (b) MRI: significant venous leakage (mixed type) is visualized, including a caverno-balanic shunt. ANOVA IRM - Germany
ANOVA IRM Treatment Approach for Erectile Dysfunction
At ANOVA IRM, ED treatment is planned within a regulated German medical setting and begins with a review of the diagnostic findings, medical history and previous treatment response.
ANOVA uses autologous treatment concepts derived from the patient's own biological material. For ED, the current approach primarily focuses on cell-free Mesenchymal Stem Cell Secretome / Exosome therapy, also known as MSEC therapy. Depending on the diagnostic findings and physician assessment, Bone Marrow Concentrate (BMC) may be used as a standalone treatment or combined with MSEC.
What Therapeutic Outcomes Can Be Expected?
Treatment goals are individualized and monitored through clinical, functional and imaging-related measures.
Potential treatment goals or monitoring areas may include:
- Ability to achieve and maintain an erection
- Penile rigidity and spontaneous or morning erections
- Response to PDE5 inhibitors or other established therapies
- Validated erectile-function scores
- Penile blood-flow findings, sexual satisfaction and quality of life
The relevance of each goal depends on the cause and extent of the patient's ED.
Potency Hypothesis of Stem Cell Therapies
Mesenchymal stem cells communicate with nearby cells through substances they release, a process commonly described as paracrine signalling. In ED research, this signalling is being studied in relation to endothelial function, cavernosal nerve support, smooth-muscle survival, inflammation and tissue remodelling.
The stem cell secretome contains exosomes and other extracellular vesicles, growth factors, cytokines, proteins and microRNAs. Earlier research involving living-cell therapies has also considered engraftment and cellular differentiation, but those mechanisms do not apply to a cell-free product.
ANOVA's MSEC rationale therefore focuses on whether factors released by mesenchymal stem cells may influence the tissue environment involved in physical ED.
MSEC / Mesenchymal Stem Cell Secretome / Exosome-Containing Therapy
Mesenchymal Stem Cell Secretome, or MSEC, is a cell-free, exosome-containing treatment derived from cultivated mesenchymal stem cells. It uses the substances released by the cells rather than transplanting the living cells themselves.
At ANOVA IRM, MSEC is produced from the patient's own adipose-derived mesenchymal stem cells. A limited amount of abdominal fat is collected through mini-liposuction under light sedation. The cells are then cultivated, and the substances they release are separated from the living MSCs and quality-controlled.
A practical advantage of MSEC is that it can be frozen and stored for later applications. One mini-liposuction generally provides 10 planned MSEC doses that can be administered over a longer treatment period within the stored shelf life of two years. This avoids repeating the tissue collection for every treatment visit.
The timing and method of applications depend on the individual treatment plan.
Learn more about ANOVA IRM’s Secretome / Exosome therapies.
Who May Be a Candidate for Erectile Dysfunction Stem Cell Therapy?
As an experimental treatment, MSEC therapy is not suitable for every patient with erectile dysfunction.
ANOVA considers MSEC therapy for selected patients whose ED has a suspected or confirmed physical component. Suitability is determined through an individual medical review.
Patients who may be considered include those with:
- Persistent ED with a suspected or confirmed physical component
- Vasculogenic or neurogenic ED
- Diabetic erectile dysfunction or ED associated with another metabolic condition
- Post-prostatectomy erectile dysfunction or ED following another pelvic treatment, where medically appropriate
- ED following relevant penile or pelvic trauma
- Persistent symptoms despite established treatment or inability to use suitable established options
- Medical suitability for the collection and application procedures required by the proposed treatment plan
- Ability to travel to Offenbach, Germany, for evaluation and treatment
ANOVA IRM does not treat patients when the following contraindications apply:
- Active cancer within the last two years
- Not being of legal age
- Inability to breathe independently or ventilator dependence
- Difficulty breathing while lying down
- Dysphagia or extreme difficulty swallowing
- Psychiatric disorder
- Active infectious disease, including hepatitis A, B or C, HIV, syphilis or another active infection

MSC secretome - exosome - therapy
ANOVA IRM - Germany
Therapy Workflow for Erectile Dysfunction
What to Expect From the Treatment Process
The treatment pathway depends on whether the individual plan includes MSEC, BMC alone or a combination of both. ANOVA confirms the applicable preparation and scheduling requirements before treatment.
Step 1: Remote Erectile Dysfunction Inquiry Review
For international patients, the process normally begins remotely. After the patient submits ANOVA IRM's contact form, the patient care team explains the treatment concept and the information required for review.
A video consultation with Dr. Michael K. Stehling may then be arranged. ANOVA reviews the patient's ED history, current care and available diagnostic findings to determine whether an in-person assessment is appropriate.
Step 2: Pre-Treatment Eligibility Testing and Day-One Confirmation
Once initial suitability appears possible, ANOVA IRM generally recommends preliminary bloodwork in the patient's home country before travel. This helps identify exclusion criteria such as HIV, hepatitis A, B or C, syphilis or another active infectious disease and reduces the risk of unnecessary travel. Certain medical or substance-use risk factors may also prevent treatment.
If the preliminary results do not show an exclusion criterion, the patient can travel to ANOVA IRM in Offenbach. On the first day, ANOVA repeats the required bloodwork as part of its eligibility and processing protocol.
ANOVA also reviews the ED-specific diagnostic findings described above and may complete additional bloodwork or penile imaging where needed. This work-up helps identify the probable cause and severity of ED and informs whether MSEC therapy may be medically appropriate.
Treatment can proceed only after the physician confirms eligibility and determines that the individual assessment supports treatment.
Step 3: Erectile Dysfunction Treatment Planning
ANOVA develops an individualized application schedule after reviewing the patient's diagnostic findings, medical history and previous treatment response. Overall health and travel requirements are also considered.
Standard protocol patterns may provide a starting framework:
- Intense: Applications occur in closer succession and may be considered for more acute ED cases or when a compressed schedule is medically appropriate.
- Balanced-Boost: Applications are distributed over a longer period and may be considered for chronic ED or patients with limited travel availability.
These are examples rather than fixed schedules. The physician adjusts the timing and distribution of doses according to the individual treatment plan.
ANOVA reviews the proposed schedule, travel requirements and estimated cost with the patient before treatment proceeds.
Step 4: Treatment Preparation
After evaluation, ANOVA confirms whether treatment will involve MSEC, BMC alone or a combination of both.
Treatment involving MSEC
The initial visit to Offenbach generally requires approximately two consecutive days. Required testing and medical confirmation take place on the first day, with mini-liposuction usually planned for the following day.
A limited amount of abdominal fat is collected under light sedation. Mesenchymal stem cells are isolated from the adipose tissue and cultivated so that the substances they release can be used to produce the patient's MSEC.
The final preparation no longer contains living MSCs. Production and quality control take approximately four weeks, and the patient does not need to remain in Germany during this period.
BMC-only treatment
Bone marrow is collected and processed without mini-liposuction or the four-week MSEC production period. Depending on the individual schedule, BMC collection and application may be completed without a return visit.
When BMC and MSEC are combined, ANOVA coordinates both procedures within the individual treatment plan.
Step 5: MSEC Applications, If Included
If the treatment plan includes MSEC, the patient returns to Offenbach after production is complete. Applications follow the individualized schedule established during treatment planning.
Any stored MSEC doses must be used within the two-year storage period. Further MSEC treatment beyond the available doses or storage period would require another medical review and tissue collection.
Treatment Timeline and Travel Requirements
Initial analysis and counselling can normally begin remotely. The in-person MSEC process is then built around three stages:
- Eligibility testing and mini-liposuction: Approximately two consecutive days in Offenbach
- MSEC production: Approximately four weeks, during which the patient can return home
- MSEC applications: Return visits to Offenbach according to the individual treatment plan, with any stored doses used within two years
Patients receiving BMC alone may not require a return visit. For combined BMC and MSEC treatment, ANOVA confirms the procedural and travel schedule individually.
The number and timing of return visits depend on the treatment plan and the patient's travel distance. International patients receiving MSEC should expect repeated travel if they intend to complete all planned applications.
Cost of Stem Cell Therapy for Erectile Dysfunction
MSEC treatment generally costs approximately €20,000 to €36,000, depending on the total number of doses used.
Costs for BMC alone or combined BMC and MSEC treatment are determined individually.
ANOVA IRM provides an individualized estimate before treatment. International patients should budget separately for travel and accommodation.
Does Health Insurance Cover the Therapy Costs?
Experimental MSEC therapy and BMC treatment included in an individual ED treatment plan are generally not covered by health insurance.
Patients should expect to pay for treatment themselves unless their insurer confirms otherwise. Insurance coverage should not be assumed.
Why Choose ANOVA IRM for Erectile Dysfunction Treatment?
- Cause-focused medical assessment: ANOVA reviews physical, psychological and mixed contributors before a treatment approach is selected.
- Specialized ED diagnostics: ANOVA typically recommends SKAT-MRI, a penile MRI performed during a pharmacologically induced erection, to evaluate structural and vascular contributors to ED.
- Autologous MSEC production: ANOVA produces MSEC from the patient's own adipose-derived mesenchymal stem cells rather than donor-derived material.
- Cell-free MSEC concept: The final MSEC preparation contains secreted factors rather than living MSCs.
- Imaging-informed treatment planning: ANOVA uses diagnostic imaging findings to identify probable anatomical contributors and guide individualized treatment planning.
- Controlled treatment in Germany: Treatment takes place at ANOVA IRM in Offenbach within a regulated medical setting and includes product quality controls.
- Individual treatment planning: Diagnostic findings, established care, eligibility, travel, cost and experimental status are reviewed before treatment.
Request a Medical Evaluation
Find out whether ANOVA's stem cell-based approach may be medically appropriate for your type of erectile dysfunction.
ANOVA IRM can begin with a remote medical review before you travel to Germany. The patient care team can explain what information is needed, outline the next steps and help arrange a physician consultation.
Treatment is considered after an individual medical review of the ED diagnosis, underlying contributors, previous care and procedural suitability.
Contact ANOVA IRM to begin your confidential remote medical evaluation.
Frequently Asked Questions About Stem Cell Therapy for Erectile Dysfunction
Is Stem Cell Therapy for Erectile Dysfunction Available at ANOVA IRM?
Yes. ANOVA IRM evaluates selected patients for experimental autologous MSEC therapy. Depending on the diagnostic findings and physician assessment, BMC may be used as a standalone treatment or combined with MSEC.
The process begins with a medical review to identify the probable cause of ED and determine whether further assessment may be appropriate.
Does Stem Cell Therapy Work for Erectile Dysfunction?
Stem cell-based treatment for ED remains under investigation. Laboratory and animal studies have reported effects on vascular, nerve and erectile-tissue pathways, while small early human studies of several living-cell products have reported encouraging findings in some patient groups.
Because these studies used different cell products, treatment methods and patient populations, the results remain preliminary. They provide scientific background for regenerative approaches to ED but are not direct evidence for ANOVA's cell-free MSEC therapy.
Who May Be a Candidate for ED Stem Cell Therapy?
ANOVA may consider selected patients with persistent ED and a suspected or confirmed physical component, including vascular, neurological, metabolic, postsurgical or trauma-related factors. Suitability also depends on overall health, previous treatment, diagnostic findings and procedural safety.
Can MSEC Therapy Help ED After Prostate Cancer Treatment?
ED following prostate surgery or radiation may involve nerve, vascular and erectile-tissue changes that are relevant to regenerative research.
ANOVA must review the patient's diagnosis, previous cancer treatment, current cancer status and the clinic's cancer-related eligibility requirements before treatment can be considered.
What Is MSEC / Stem Cell Secretome Therapy?
MSEC stands for Mesenchymal Stem Cell Secretome. It is a cell-free, exosome-containing preparation composed of substances released by mesenchymal stem cells.
At ANOVA IRM, MSEC is produced using the patient's own adipose-derived mesenchymal stem cells. The final preparation contains the substances released by those cells rather than living MSCs.
Does MSEC Replace Viagra, Cialis or Other ED Treatments?
No. PDE5 inhibitors, management of contributing health conditions, psychological care, vacuum devices, injectable medication or a penile prosthesis may remain appropriate.
MSEC may be considered alongside established care within an individualized treatment plan. Patients should not stop prescribed ED treatment without consulting their physician.
Can International Patients Apply for Treatment?
Yes. The initial medical review and physician consultation can usually begin remotely. Travel to Offenbach, Germany, is required for final assessment and treatment. Patients receiving MSEC return for subsequent applications according to the individual plan.
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Further References for MSC, BMC, Stemcell Secretome and EVs
- Georg Hansmann, Philippe Chouvarine, Franziska Diekmann, Martin Giera, Markus Ralser, Michael Mülleder, Constantin von Kaisenberg, Harald Bertram, Ekaterina Legchenko & Ralf Hass "Human umbilical cord mesenchymal stem cell-derived treatment of severe pulmonary arterial hypertension". Nature Cardiovascular Research volume 1, pages568–576 (2022).
- Murphy JM, Fink DJ, Hunziker EB, et al. Stem cell therapy in a caprine model of osteoarthritis . Arthritis Rheum. 2003;48:3464–74.
- Lee KB, Hui JH, Song IC, Ardany L, et al. Injectable mesenchymal stem cell therapy for large cartilage defects—a porcine model. Stem Cell. 2007;25:2964–71.
- Saw KY, Hussin P, Loke SC, et al. Articular cartilage regeneration with autologous marrow aspirate and hyaluronic acid: an experimental study in a goat model. Arthroscopy . 2009;25(12):1391–400.
- Black L, Gaynor J, Adams C, et al. Effect of intra-articular injection of autologous adipose-derived mesenchymal stem and regenerative cells on clinical signs of chronic osteoarthritis of the elbow joint in dogs. Vet Ther. 2008;9:192-200.
- Centeno C, Busse D, Kisiday J, et al. Increased knee cartilage volume in degenerative joint disease using percutaneously implanted, autologous mesenchymal stem cells. Pain Physician. 2008;11(3):343–53.
- Centeno C, Kisiday J, Freeman M, et al. Partial regeneration of the human hip via autologous bone marrow nucleated cell transfer: a case study. Pain Physician. 2006;9:253–6.
- Centeno C, Schultz J, Cheever M. Safety and complications reporting on the re-implantation of culture-expanded mesenchymal stem cells using autologous platelet lysate technique. Curr Stem Cell. 2011;5(1):81–93.
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- Kuroda R, Ishida K, et al. Treatment of a full-thickness articular cartilage defect in the femoral condyle of an athlete with autologous bone-marrow stromal cells. Osteoarthritis Cartilage. 2007;15:226–31.
- Emadedin M, Aghdami N, Taghiyar L, et al. Intra-articular injection of autologous mesenchymal stem cells in six patients with knee osteoarthritis. Arch Iran Med. 2012;15(7):422–8.
- Saw KY et al. Articular cartilage regeneration with autologous peripheral blood stem cells versus hyaluronic acid: a randomized controlled trial. Arthroscopy. 2013;29(4):684–94.
- Vangsness CT, Farr J, Boyd J, et al. Adult human mesenchymal stem cells delivered via intra-articular injection to the knee following partial medial meniscectomy. J Bone Joint Surg. 2014;96(2):90–8.
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Further References about PRP
- Rubio-Azpeitia E, Andia I. Partnership between platelet-rich plasma and mesenchymal stem cells: in vitro experience. Muscles Ligaments Tendons J. 2014;4(1):52–62.
Extras
- Xu, Ming, et al. " Transplanted senescent cells induce an osteoarthritis-like condition in mice. " The Journals of Gerontology Series A: Biological Sciences and Medical Sciences (2016): glw154.
- McCulloch, Kendal, Gary J. Litherland, and Taranjit Singh Rai. " Cellular senescence in osteoarthritis pathology ." Aging Cell (2017).
Contraindications
Our stem cell treatments are experimental, but we only treat patients for whom we believe the risk/benefit ratio indicates treatment based on the state of the art, i.e., medical, scientific evidence.
Please understand that we therefore do not treat patients for whom the following points apply:
- Active cancer in the last two years
- Not yet of legal age
- Existing pregnancy or lactation period
- Unable to breathe on own, ventilator
- Difficulty breathing in supine position
- Dysphagia (extreme difficulty swallowing)
- Psychiatric disorder
- Active infectious disease (Hepatitis A, B, C, HIV, Syphilis, or other)