Umbilical Cord-Derived Mesenchymal Stem Cell (VCELL 1) for Male Patients With Sexual Deficiency
- Conditions
- Sexual Dysfunction Male
- Interventions
- Biological: Umbilical Cord-Derived Mesenchymal Stem Cell for Male Patients with Sexual Deficiency
- Registration Number
- NCT05345418
- Brief Summary
Sexual functional deficiency affects largely the physical conditions, life and sexual quality of the patients. Hypogonadism affects about 4 to 5 million men in the US, and the incidence increases with age. In our recent phase I clinical trial, we have shown that intravenous adipose - derived MSC administration was safe in female and male patients with hormone deficiency. Post-transplantation sexual satisfaction was observed in all patients enrolled in this study. Testosterone levels in males increased significantly after transplantation and were maintained at high levels for up to 6 months before decreasing again at the 12-month follow-up. The aim of this clinical trial was to assess the safety and effectiveness of allogeneic administration of MSCs in middle-aged people with sexual functional deficiency.
- Detailed Description
Sexual functional deficiency occurs at some point in life and becomes a problematic issue in middle-aged adulthood. Regenerative medicine, especially mesenchymal stem cell (MSC) transplantation, has developed extensively, with preclinical and clinical trials emphasizing the benefits of stem cell therapy for restoration of sexual deficiency. n our recent phase I clinical trial, we have shown that intravenous adipose - derived MSC administration was safe in female and male patients with hormone deficiency. Post-transplantation sexual satisfaction was observed in all patients enrolled in this study. Testosterone levels in males increased significantly after transplantation and were maintained at high levels for up to 6 months before decreasing again at the 12-month follow-up. The aim of this clinical trial was to assess the safety and effectiveness of allogeneic administration of MSCs in middle-aged people with sexual functional deficiency. In phase II, 40 males with hormone deficiency will be recruited and divided randomly into two groups (n=23 each). The group A will receive UC-MSCs intravenously at day 0 and day 90 ± 7, while the group B will be infused with UC-MSCs at day 180 ± 14 and day 270 ± 14. Each group will be monitored for 365 ± 14 days after the first infusion. The phase II is to investigate safety and efficacy of UC-MSC infusion for the treatment of sexual hormone deficiency in males.
The primary outcome are: (1) numbers of AEs or SAEs during UC-MSC infusion and 365 ± 14 days after the first infusion; (2) Testosterone levels and sexual life quality through quantification of Aging Men Symptom (AMS), International Index of Erectile Function (IIEF), and Sexual Quality of Life Questionnaire (SQoL-M) at day 90 ± 7 and day 180 ± 14 of the group A compared to those of the group B.
The secondary outcome are: (1) Testosterone levels and (2) sexual life quality through quantification of AMS, IIEF, and SQoL-M at day 90 ± 7, day 180 ± 14, and day 365 ± 14 after the first UC-MSC infusion of each group compared to the baseline; (3) cytokine concentration (TNFa, IFN-γ, IL1, IL-6, IL-8, IL-4, IL-10, IDO) in serum of the participants and their T cell immunophenotype at day 90 ± 7, day 180 ± 14, and day 365 ± 14 after the first UC-MSC infusion.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Male
- Target Recruitment
- 158
- Males with sexual hormone deficiency aged 50 to 70 years
- AMS score ≥ 27
- IIEF < 14
- SQoL-M ≤ 87
- and Testosterone ≤ 12 nMol/L
- Normal liver function (ALT, AST and Bilirubin are normal according to biological index of Vietnamese people).
- Normal kidney function is usually according to the biological index of Vietnamese people.
- No infection, HIV, HBV, active syphilis.
- Must provide written informed consent.
- The patient had surgery to remove the gonads.
- Patients with a history of cancer, or undergoing cancer treatment, or are positive for cancer screening tests including: PSA, AFP, Pepsinogen I, Pepsinogen II and erythrocyte smear test.
The patient is taking anti-rejection drugs.
- Patients with malformations, malformations or tumors of the endocrine glands.
- Endocrine impairment due to diabetes (HBA1c > 7) and other metabolic diseases.
- Patients with active autoimmune disease or positive for antinuclear antibodies.
- Patients with severe heart failure, severe renal failure, severe liver failure, severe respiratory failure, history of cerebral infarction, myocardial infarction, Alzeimer.
- Patients with hypothyroidism.
- The patient has an acute infection.
- Patients with clinically significant coagulopathy or other hematological diseases.
- History of allergy to anesthetics, anesthetics, antibiotics.
- Patients who are using other hormone-improving drugs or supplements (including Sildenafil) in the last 2 weeks or want to continue using these drugs during the study period.
- The patient is a smoker.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Umbilical Cord-Derived Mesenchymal Stem Cell, then Placebo (group A) Umbilical Cord-Derived Mesenchymal Stem Cell for Male Patients with Sexual Deficiency Cohort 1 will receive two single intravenous dose of UC MSCs of 1.5 million cells per kilogram body weight on their Study Month 0, and Study Month 3. - Each treatment period was separated by a 4 - week washout to allow the effective systemic elimination of the UC MSCs before subsequent treatment initiation Placebo, then Umbilical Cord-Derived Mesenchymal Stem Cell (group B) Umbilical Cord-Derived Mesenchymal Stem Cell for Male Patients with Sexual Deficiency Cohort 2 will receive two single intravenous dose of UC MSCs of 1.5 million cells per kilogram body weight on their Study Month 7, and Study Month 10
- Primary Outcome Measures
Name Time Method Changes in sexual life quality through quantification of International Index of Erectile Function (IIEF) up to the 12-month period following treatment IIEF includes 15 items
Changes in sexual life quality using Aging Men Symptom (AMS) up to the 12-month period following treatment AMS includes 10 items
Changes in sexual life quality through quantification of Sexual Quality of Life Questionnaire (SQoL-M) up to the 12-month period following treatment IIEF includes 11 items
Testosterone levels up to the 12-month period following treatment To evaluate the Testosterone levels of the patients with sexual functional deficiency
The safety of allogenic umbilical cord-derived mesenchymal stem cell administration for the treatment of hormone deficiency in male up to the 12-month period following treatment To assess safety, the number of AEs or SAEs during stem cell administration up to the 12-month period following treatment will be evaluated
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Vinmec Research Institute of Stem Cell and Gene Technology
🇻🇳Hanoi, Vietnam