Gonadal DysfunctionFERTILENCT06841328
Fertility Enhancement Through Regenerative Treatment in Ovaries and Testes
An observational study of Gonadal Dysfunction and Gonadal Failure, run by Jumeirah American Clinic at 1 site in United Arab Emirates.
Trial summary
This study investigates the safety and efficacy of stem cell or stem cell-derived exosome therapy for gonadal failure, including testicular failure, hypogonadism, ovarian insufficiency, and premature ovarian failure (POF). Read more about this study
- Who is it for?
- Ages 20 to 50 years
- Conditions the study is for
- Gonadal Dysfunction, Gonadal Failure, Azoospermia
- What is being tested?
- Stem cells
- Type of treatment
- Injection or infusion, Surgery or procedure
- How many people
- 60 participants
- Where
- 1 siteUnited Arab Emirates
- Study dates
- 8 Apr 2025to 30 Apr 2028
- How long will I take part?
- 12 Months
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 50 years
- All sexes
- No healthy volunteers
- Adult
Study population: The study population will consist of adult male and female patients aged 20 to 50 years who are diagnosed with testicular or ovarian failure and are seeking treatment at First IVF and Day Surgery Center. Participants will be recruited from the pool of patients under the care of the PI or the co-Is. Eligibility will include individuals with confirmed testicular or ovarian failure based on clinical, hormonal, and imaging criteria who have not responded adequately to conventional treatments such as hormone therapy (HT).
Who may be able to join
None listed.
Who cannot join
- Severe comorbid conditions, such as advanced cardiovascular disease, renal failure, or uncontrolled diabetes.
- Active malignancies or history of cancer within the past 5 years.
- Active infections or systemic inflammatory conditions.
- History of testicular surgery or trauma that could interfere with the study outcomes.
- Use of anticoagulants or medications that may contraindicate stem cell or stem cell-derived exosome therapy.
- Participation in another investigational drug or treatment study within the past 6 months.
Show all 11Show fewer
- Contraindications to stem cell or stem cell-derived exosome therapy, such as immune deficiencies or allergies to any treatment components.
- Severe neurological disorders or cognitive impairment may limit the ability to provide informed consent or follow study instructions.
- Any condition that, in the investigator's opinion, could interfere with the study or pose an undue risk to the patient.
- Women with a primary diagnosis of psychogenic ovarian dysfunction or infertility.
- History of ovarian surgery or trauma that could interfere with the study outcomes.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Sheila May, RN contact
United Arab Emirates1 site, 1 recruiting
- Recruiting
First IVF and Day Surgery Center
Dubai, Dubai
Sheila May, RN, +971 4 770 1741, may.jesus@firstivf.ae
Zaed Jaber, zaed.jaber@students.mbru.ac.ae
About this study
Official title: Fertility Enhancement Through Regenerative Treatment in Ovaries and Testes: (FERTILE): Prospective Observational Study Evaluating Safety and Efficacy
This study investigates the safety and efficacy of stem cell or stem cell-derived exosome therapy for gonadal failure, including testicular failure, hypogonadism, ovarian insufficiency, and premature ovarian failure (POF). Conducted at First IVF Clinic, Dubai, it will include 60 participants (30 males, 30 females) aged 20-50 years who have not responded to conventional treatments such as HRT, TRT, or ART.
Participants will receive intra-gonadal (testicular or ovarian) injections of stem cells or exosomes, with follow-ups at 3, 6, 9, and 12 months to monitor hormonal changes, gonadal function, and potential adverse effects. The study aims to determine whether regenerative therapy can restore hormone production, enhance reproductive function, and regenerate gonadal tissue, providing a novel, culturally appropriate fertility treatment in the UAE, where donor sperm and eggs are not permitted.
By bridging the gap between preclinical research and clinical application, this study could offer new hope to individuals with gonadal failure, advancing the field of regenerative reproductive medicine.
Read the detailed description
Background and Rationale:
Testicular and ovarian failure, often called 'gonadal failure,' occurs when the testes or ovaries lose their ability to produce gametes. Both lead to reduced fertility and hormonal deficiencies, significantly impacting an individual's health and quality of life. Conventional treatments such as hormone replacement therapy (HRT) help alleviate symptoms but do not restore fertility.
Surgical options (testicular sperm retrieval, ultrasound-guided egg retrieval) are found to be helpful for some. However, they are not uniformly successful 11. Surgeries (testicular biopsies) always carry risks such as risk of bleeding or infection and lack of guaranteed success 12. Clinicians are exploring less invasive alternatives like stem cell-based therapies, including adipose-derived stem cells (ADSCs) and exosomes. Stem cells or stem cell-derived exosome therapy offers a promising regenerative approach for restoring gonadal function by enhancing tissue repair, stimulating folliculogenesis or spermatogenesis, modulating hormonal balance, and improving overall reproductive potential in individuals with testicular or ovarian failure.
This study assesses the safety and efficacy of intra-gonadal (testicular or ovarian) stem cells or stem cell-derived exosome injection for patients with testicular and ovarian failure who have not responded to conventional treatments. ADSC therapy has been studied in humans for related conditions like ovarian insufficiency and POF (Premature ovarian failure)6. It has shown encouraging results in repairing damaged tissues and improving hormonal function, showing early successes that provide hope for its potential. This research assumes even greater importance in the UAE, where donor sperm and eggs are not permitted due to religious and legal restrictions 13. Testing the safety and long-term efficacy of ADSC therapy for gonadal failure in the UAE could provide a groundbreaking, culturally appropriate solution for individuals facing reproductive challenges, giving them new opportunities for treatment and a renewed sense of hope.
The Bioscience Institute, a DHA-approved facility, will provide the stem cells or stem cell-derived exosomes under an existing Memorandum of Understanding (MOU) with the First IVF Clinic and Day Surgery Center. The stem cells or stem cell-derived exosomes will be extracted and produced in an off-site laboratory (Bioscience Institute) and undergo sterility, cell count, and viability check before being prepared for administration back into the patient. The manufacturing process follows CGTP. The cells will be injected directly into the testes and ovaries under anesthesia.
Study Objectives
- Primary Objective:
- To evaluate the safety and efficacy of intraovarian or intratesticular injections of stem cells or stem cell-derived exosomes in restoring gonadal function, as measured by hormonal changes (testosterone, estradiol, FSH, AMH) and reproductive capacity from baseline to post-treatment.
- Secondary Objectives:
- Assess gonadal tissue regeneration using imaging techniques.
- Monitor long-term treatment effects at follow-up points
- Document any adverse events or complications related to stem cell or exosome therapy, such as fibrosis, infection, or immune reactions.
- Evaluate functional outcomes such as spermatogenesis in men (via semen analysis) and ovarian follicular activity in women (via antral follicle count and menstrual cycle regularity).
- Compare the effects of stem cells vs. stem cell-derived exosomes in improving gonadal function and hormone levels.
Study Design and Objectives This open-label, single-arm, pilot observational study will serve as a preliminary investigation into the use of adipose-derived stem cells (ADSCs) or stem cell-derived exosomes for treating gonadal failure in both men and women. The study's primary focus will be on assessing safety and feasibility, while also gathering initial efficacy data to support future large-scale trials.
Study Population The study will enroll 60 adults (30 males, 30 females) aged 20 to 50 years diagnosed with gonadal failure, including testicular failure, hypogonadism, ovarian insufficiency, or premature ovarian failure (POF). Participants must have failed or experienced suboptimal responses to conventional treatments, such as hormone replacement therapy (HRT), testosterone replacement therapy (TRT), or assisted reproductive technologies (ART).
Recruitment will take place at First IVF Clinic, Dubai, where participants are actively receiving evaluation and treatment for gonadal failure. The inclusion and exclusion criteria will ensure that the study targets individuals most likely to benefit from therapy while prioritizing patient safety.
Sample Size Rationale A sample size of 60 participants was selected based on the exploratory nature of the study. The primary objective is to assess the feasibility, safety, and preliminary efficacy of stem cell or exosome therapy while providing sufficient data to inform the design of future, larger trials. Given the clinic's patient population, recruiting 60 participants over the planned two-year study period is considered achievable.
Study Procedures
- Informed Consent Participants will receive detailed information about the study, including its risks and potential benefits, and will provide written consent prior to enrollment.
- Baseline Assessments Before treatment, participants will undergo comprehensive baseline testing, including: Hormonal blood tests (Testosterone, Estradiol, FSH, AMH) Ultrasound imaging (AFC for ovaries, testicular volume for testes) Semen analysis (for male participants, if applicable) Medical history review and general health evaluation
- Therapeutic Administration For ADSCs: ADSCs will be harvested via minimally invasive liposuction from the participant's own adipose tissue. The cells will be processed, purified, and prepared for injection into the ovaries (females) or testes (males). For Exosomes: Exosomes will be derived from stem cells, isolated, and purified before administration. The injections will follow the same procedure as stem cell therapy, ensuring targeted delivery into the gonads. Injection Procedure: Ovarian injections: Administered via direct intraovarian injection. Testicular injections: Administered via direct intratesticular injection in rete testis.
- Follow-Up Monitoring
Participants will be monitored immediately post-injection for any adverse reactions and will return for regular follow-ups at 3, 6, 9, and 12 months to assess:
Data Collection and Analysis Collected data will be analyzed to evaluate primary and secondary outcomes.
Primary Outcome:
Hormonal level changes from baseline to 12 months post-treatment.
Secondary Outcomes:
Changes in gonadal tissue structure (AFC, testicular volume). Functional improvements (spermatogenesis, menstrual cycle regulation). Incidence of adverse events (infection, fibrosis, immune response). Surgical sperm retrieval and Egg retrieval success
Ethical Considerations This study will adhere to strict ethical standards for clinical research.
Ethics Committee Review: The protocol will be reviewed and approved by an independent ethics board.
Informed Consent: Participants will have full autonomy to decide on participation and may withdraw at any time without affecting their standard medical care.
Confidentiality: All patient data will be anonymized and stored securely to ensure privacy.
Expected Outcomes
This study aims to provide early evidence on the safety and potential efficacy of stem cell or exosome therapy for gonadal failure. If successful, participants are expected to show:
Improvements in hormone levels and reproductive function. Gonadal tissue regeneration, restoring follicular activity or spermatogenesis. Minimal adverse effects, confirming safety and feasibility. The findings from this study will help guide future, larger-scale trials and contribute to the development of regenerative therapies for gonadal failure, offering a novel and culturally appropriate solution for fertility preservation in the UAE.
- Conditions
- Gonadal Dysfunction, Gonadal Failure, Azoospermia, Testosterone Deficiency, Stem Cells, Hypogonadism, Male
- Being tested
- Stem cells
- Keywords
- Premature Ovarian Failure, Testicular Failure, low testosterone, Stem cell therapy, Exosomes
- Medical subject headings
- Gonadal Disorders, Azoospermia, Eunuchism, Primary Ovarian Insufficiency
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Stem cellsProcedure or surgery
The administration of stem cell or stem cell-derived exosome therapy as a regenerative treatment for gonadal failure in both men and women. The intervention involves a single intra-gonadal injection (testicular or ovarian) of adipose-derived stem cells (ADSCs) or exosomes.
| Study group | Role | What they receive |
|---|---|---|
| Male | Male patients aged 20 to 50 years. Diagnosed with testicular failure (low testosterone) or hypogonadism (impaired gonadal function), or azoospermia due to production defect (no sperm in ejaculate) Receives: Procedure: Stem cells | |
| Female | Female patients aged 20 to 50 years. Diagnosed with premature ovarian failure (POF) or ovarian insufficiency, confirmed through clinical, hormonal, and imaging assessments. Receives: Procedure: Stem cells |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in reproductive capacity
We will evaluate hormonal changes (testosterone, estradiol, FSH, AMH) and sperm parameters
Measured: 12 months
Secondary outcomes (1)
Gonadal Function
Evaluate functional outcomes such as surgical sperm retrieval success and ovarian follicular activity in women (via antral follicle count and egg retrieval success)
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Feb 2025
- Study start8 Apr 2025
- Primary completion30 Apr 2027 (estimated)
- Study completion30 Apr 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Gonadal DysfunctionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 60 participants (estimated)
- Target duration
- 12 Months
Sponsor and investigators
- Lead sponsor
- Jumeirah American Clinic
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ranjith Ramasamy, Jumeirah American Clinic
- Investigators
- Ranjith Ramasamy, MD, Principal investigator, Jumeirah American Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06841328
- Sponsor's protocol ID
- 002
- Acronym
- FERTILE
- Status last verified
- Apr 2025
- First submitted
- 18 Feb 2025
- Last updated
- 10 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The study will involve the collection of individual participant data (IPD) related to adult male and female patients aged 20 to 50 years diagnosed with testicular or ovarian failure who are seeking treatment at First IVF and Day Surgery Center. The specific IPD that will be shared includes: 1. De-identified Data to be Shared Demographic Data: Age, sex, and relevant medical history (without personal identifiers). Clinical Data: Diagnosis of testicular or ovarian failure, including clinical presentation and duration of symptoms. Hormonal and Imaging Data: Laboratory test results (e.g., hormone levels such as FSH, LH, testosterone, estrogen) and imaging findings confirming the diagnosis. Treatment and Response Data: Information on previous hormone therapy (HT) and response status. Outcome Measures: Treatment efficacy, adverse events, and follow-up assessments. 2. Data Not to be Shared Personal identifiers such as names, contact details, and specific identifying information.
Publications
Zafardoust S, Kazemnejad S, Darzi M, Fathi-Kazerooni M, Rastegari H, Mohammadzadeh A. Improvement of Pregnancy Rate and Live Birth Rate in Poor Ovarian Responders by Intraovarian Administration of Autologous Menstrual Blood Derived- Mesenchymal Stromal Cells: Phase I/II Clinical Trial. Stem Cell Rev Rep. 2020 Aug;16(4):755-763. doi: 10.1007/s12015-020-09969-6.
PubMed 32198596
Study at a glance
From the registry record, last updated by the sponsor on 10 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Fertility Enhancement Through Regenerative Treatment in Ovaries and Testes: (FERTILE): Prospective Observational Study Evaluating Safety and Efficacy
- ClinicalTrials.gov ID
- NCT06841328
- Acronym / sponsor ID
- FERTILE / 002
- Conditions
- Gonadal Dysfunction, Gonadal Failure, Azoospermia, Testosterone Deficiency, Stem Cells, Hypogonadism, Male
- Keywords
- Premature Ovarian Failure, Testicular Failure, low testosterone, Stem cell therapy, Exosomes
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Jumeirah American ClinicUniversity, hospital or other
- Study start
- 8 Apr 2025 (actual)
- Primary completion
- 30 Apr 2027 (estimated)
- Study completion
- 30 Apr 2028 (estimated)
- First posted
- 24 Feb 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study investigates the safety and efficacy of stem cell or stem cell-derived exosome therapy for gonadal failure, including testicular failure, hypogonadism, ovarian insufficiency, and premature ovarian failure (POF). Conducted at First IVF Clinic, Dubai, it will include 60 participants (30 males, 30 females) aged 20-50 years who have not responded to conventional treatments such as HRT, TRT, or ART.
Participants will receive intra-gonadal (testicular or ovarian) injections of stem cells or exosomes, with follow-ups at 3, 6, 9, and 12 months to monitor hormonal changes, gonadal function, and potential adverse effects. The study aims to determine whether regenerative therapy can restore hormone production, enhance reproductive function, and regenerate gonadal tissue, providing a novel, culturally appropriate fertility treatment in the UAE, where donor sperm and eggs are not permitted.
By bridging the gap between preclinical research and clinical application, this study could offer new hope to individuals with gonadal failure, advancing the field of regenerative reproductive medicine.
Detailed description
Background and Rationale:
Testicular and ovarian failure, often called 'gonadal failure,' occurs when the testes or ovaries lose their ability to produce gametes. Both lead to reduced fertility and hormonal deficiencies, significantly impacting an individual's health and quality of life. Conventional treatments such as hormone replacement therapy (HRT) help alleviate symptoms but do not restore fertility.
Surgical options (testicular sperm retrieval, ultrasound-guided egg retrieval) are found to be helpful for some. However, they are not uniformly successful 11. Surgeries (testicular biopsies) always carry risks such as risk of bleeding or infection and lack of guaranteed success 12. Clinicians are exploring less invasive alternatives like stem cell-based therapies, including adipose-derived stem cells (ADSCs) and exosomes. Stem cells or stem cell-derived exosome therapy offers a promising regenerative approach for restoring gonadal function by enhancing tissue repair, stimulating folliculogenesis or spermatogenesis, modulating hormonal balance, and improving overall reproductive potential in individuals with testicular or ovarian failure.
This study assesses the safety and efficacy of intra-gonadal (testicular or ovarian) stem cells or stem cell-derived exosome injection for patients with testicular and ovarian failure who have not responded to conventional treatments. ADSC therapy has been studied in humans for related conditions like ovarian insufficiency and POF (Premature ovarian failure)6. It has shown encouraging results in repairing damaged tissues and improving hormonal function, showing early successes that provide hope for its potential. This research assumes even greater importance in the UAE, where donor sperm and eggs are not permitted due to religious and legal restrictions 13. Testing the safety and long-term efficacy of ADSC therapy for gonadal failure in the UAE could provide a groundbreaking, culturally appropriate solution for individuals facing reproductive challenges, giving them new opportunities for treatment and a renewed sense of hope.
The Bioscience Institute, a DHA-approved facility, will provide the stem cells or stem cell-derived exosomes under an existing Memorandum of Understanding (MOU) with the First IVF Clinic and Day Surgery Center. The stem cells or stem cell-derived exosomes will be extracted and produced in an off-site laboratory (Bioscience Institute) and undergo sterility, cell count, and viability check before being prepared for administration back into the patient. The manufacturing process follows CGTP. The cells will be injected directly into the testes and ovaries under anesthesia.
Study Objectives
- Primary Objective:
- To evaluate the safety and efficacy of intraovarian or intratesticular injections of stem cells or stem cell-derived exosomes in restoring gonadal function, as measured by hormonal changes (testosterone, estradiol, FSH, AMH) and reproductive capacity from baseline to post-treatment.
- Secondary Objectives:
- Assess gonadal tissue regeneration using imaging techniques.
- Monitor long-term treatment effects at follow-up points
- Document any adverse events or complications related to stem cell or exosome therapy, such as fibrosis, infection, or immune reactions.
- Evaluate functional outcomes such as spermatogenesis in men (via semen analysis) and ovarian follicular activity in women (via antral follicle count and menstrual cycle regularity).
- Compare the effects of stem cells vs. stem cell-derived exosomes in improving gonadal function and hormone levels.
Study Design and Objectives This open-label, single-arm, pilot observational study will serve as a preliminary investigation into the use of adipose-derived stem cells (ADSCs) or stem cell-derived exosomes for treating gonadal failure in both men and women. The study's primary focus will be on assessing safety and feasibility, while also gathering initial efficacy data to support future large-scale trials.
Study Population The study will enroll 60 adults (30 males, 30 females) aged 20 to 50 years diagnosed with gonadal failure, including testicular failure, hypogonadism, ovarian insufficiency, or premature ovarian failure (POF). Participants must have failed or experienced suboptimal responses to conventional treatments, such as hormone replacement therapy (HRT), testosterone replacement therapy (TRT), or assisted reproductive technologies (ART).
Recruitment will take place at First IVF Clinic, Dubai, where participants are actively receiving evaluation and treatment for gonadal failure. The inclusion and exclusion criteria will ensure that the study targets individuals most likely to benefit from therapy while prioritizing patient safety.
Sample Size Rationale A sample size of 60 participants was selected based on the exploratory nature of the study. The primary objective is to assess the feasibility, safety, and preliminary efficacy of stem cell or exosome therapy while providing sufficient data to inform the design of future, larger trials. Given the clinic's patient population, recruiting 60 participants over the planned two-year study period is considered achievable.
Study Procedures
- Informed Consent Participants will receive detailed information about the study, including its risks and potential benefits, and will provide written consent prior to enrollment.
- Baseline Assessments Before treatment, participants will undergo comprehensive baseline testing, including: Hormonal blood tests (Testosterone, Estradiol, FSH, AMH) Ultrasound imaging (AFC for ovaries, testicular volume for testes) Semen analysis (for male participants, if applicable) Medical history review and general health evaluation
- Therapeutic Administration For ADSCs: ADSCs will be harvested via minimally invasive liposuction from the participant's own adipose tissue. The cells will be processed, purified, and prepared for injection into the ovaries (females) or testes (males). For Exosomes: Exosomes will be derived from stem cells, isolated, and purified before administration. The injections will follow the same procedure as stem cell therapy, ensuring targeted delivery into the gonads. Injection Procedure: Ovarian injections: Administered via direct intraovarian injection. Testicular injections: Administered via direct intratesticular injection in rete testis.
- Follow-Up Monitoring
Participants will be monitored immediately post-injection for any adverse reactions and will return for regular follow-ups at 3, 6, 9, and 12 months to assess:
Data Collection and Analysis Collected data will be analyzed to evaluate primary and secondary outcomes.
Primary Outcome:
Hormonal level changes from baseline to 12 months post-treatment.
Secondary Outcomes:
Changes in gonadal tissue structure (AFC, testicular volume). Functional improvements (spermatogenesis, menstrual cycle regulation). Incidence of adverse events (infection, fibrosis, immune response). Surgical sperm retrieval and Egg retrieval success
Ethical Considerations This study will adhere to strict ethical standards for clinical research.
Ethics Committee Review: The protocol will be reviewed and approved by an independent ethics board.
Informed Consent: Participants will have full autonomy to decide on participation and may withdraw at any time without affecting their standard medical care.
Confidentiality: All patient data will be anonymized and stored securely to ensure privacy.
Expected Outcomes
This study aims to provide early evidence on the safety and potential efficacy of stem cell or exosome therapy for gonadal failure. If successful, participants are expected to show:
Improvements in hormone levels and reproductive function. Gonadal tissue regeneration, restoring follicular activity or spermatogenesis. Minimal adverse effects, confirming safety and feasibility. The findings from this study will help guide future, larger-scale trials and contribute to the development of regenerative therapies for gonadal failure, offering a novel and culturally appropriate solution for fertility preservation in the UAE.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 12 Months
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Male | – | Procedure: Stem cellsMale patients aged 20 to 50 years. Diagnosed with testicular failure (low testosterone) or hypogonadism (impaired gonadal function), or azoospermia due to production defect (no sperm in ejaculate) |
| Female | – | Procedure: Stem cellsFemale patients aged 20 to 50 years. Diagnosed with premature ovarian failure (POF) or ovarian insufficiency, confirmed through clinical, hormonal, and imaging assessments. |
Who may qualify
- Ages
- 20 to 50 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- The study population will consist of adult male and female patients aged 20 to 50 years who are diagnosed with testicular or ovarian failure and are seeking treatment at First IVF and Day Surgery Center. Participants will be recruited from the pool of patients under the care of the PI or the co-Is. Eligibility will include individuals with confirmed testicular or ovarian failure based on clinical, hormonal, and imaging criteria who have not responded adequately to conventional treatments such as hormone therapy (HT).
Key inclusion criteria (0 listed)
Key exclusion criteria (11 listed)
- Severe comorbid conditions, such as advanced cardiovascular disease, renal failure, or uncontrolled diabetes.
- Active malignancies or history of cancer within the past 5 years.
- Active infections or systemic inflammatory conditions.
- History of testicular surgery or trauma that could interfere with the study outcomes.
- Use of anticoagulants or medications that may contraindicate stem cell or stem cell-derived exosome therapy.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Stem cellsThe administration of stem cell or stem cell-derived exosome therapy as a regenerative treatment for gonadal failure in both men and women. The intervention involves a single intra-gonadal injection (testicular or ovarian) of adipose-derived stem cells (ADSCs) or exosomes. | Procedure or surgery | Female, Male |
Primary outcome
Change in reproductive capacity
Time frame: 12 months
We will evaluate hormonal changes (testosterone, estradiol, FSH, AMH) and sperm parameters
1 secondary outcome
Gonadal Function
Time frame: 12 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Apr 2025.
- Background: PubMed 32198596Zafardoust S, Kazemnejad S, Darzi M, Fathi-Kazerooni M, Rastegari H, Mohammadzadeh A. Improvement of Pregnancy Rate and Live Birth Rate in Poor Ovarian Responders by Intraovarian Administration of Autologous Menstrual Blood Derived- Mesenchymal Stromal Cells: Phase I/II Clinical Trial. Stem Cell Rev Rep. 2020 Aug;16(4):755-763. doi: 10.1007/s12015-020-09969-6.
- Individual participant dataSharing planned: Yes. The study will involve the collection of individual participant data (IPD) related to adult male and female patients aged 20 to 50 years diagnosed with testicular or ovarian failure who are seeking treatment at First IVF and Day Surgery Center. The specific IPD that will be shared includes: 1. De-identified Data to be Shared Demographic Data: Age, sex, and relevant medical history (without personal identifiers). Clinical Data: Diagnosis of testicular or ovarian failure, including clinical presentation and duration of symptoms. Hormonal and Imaging Data: Laboratory test results (e.g., hormone levels such as FSH, LH, testosterone, estrogen) and imaging findings confirming the diagnosis. Treatment and Response Data: Information on previous hormone therapy (HT) and response status. Outcome Measures: Treatment efficacy, adverse events, and follow-up assessments. 2. Data Not to be Shared Personal identifiers such as names, contact details, and specific identifying information.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Sheila May, RN contact
Ranjith Ramasamy, MD principal investigator
Jumeirah American Clinic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Gonadal Dysfunction and Gonadal Failure, run by Jumeirah American Clinic at 1 site in United Arab Emirates.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 0 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 10 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Arab Emirates. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ranjith Ramasamy, MD (+971 4 770 1741, ranjith.ramasamy@jac.ae), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in reproductive capacity (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06841328, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2025.