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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05279768
Other study ID # CT/PCOS/PSI/2022
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date September 1, 2022
Est. completion date December 2023

Study information

Verified date September 2022
Source PT. Prodia Stem Cell Indonesia
Contact Gunawan Dwi Prayitno
Phone 08129004721
Email gunawan.spog04@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigating the effect of Umbilical Cord Mesenchymal Stem Cell (UC-MSCs) and secretomes to insulin resistance in Polycystic Ovary Syndrome (PCOS) patients. This study has 4 arms namely UC-MSCs treatment, secretomes treatment, UC-MSCs and secretomes treatment, and control.


Description:

The investigator hypothesized that PCOS patients with insulin resistance given combination of UC-MSCs and secretomes can improve their clinical and laboratory insulin resistance, haid ovulatory cycle and fertility. All group will be observed every 1,3, and 6 months after injection.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - PCOS patients with insulin resistance based on Rotterdam Consensus criteria, i.e. menstrual disorders (oligomenorhea/ amennorhea) - Patients must have hiperandrogenemia clinical and laboratory proof (Ferriman Gallwey score >8) - Patients with Free Androgen Index (FAI) >4 and ovary polycystic from USG transvaginal - Patients with Homeostatic (HOMA) IR score = 1.7 Exclusion Criteria: - Patients who are allergic to component of WJ-MSC or Secretome. - Patients who are not currently on hormon treatment of other resistance treatment. - Refusing or not participating in part / all of the research process. - Patients with positive diagnosis of hepatitis A,B,C, and HIV

Study Design


Intervention

Biological:
UC-MSCs
Treatment with tablet (placebo) once for 30 days, IV 0.3 million kg/bb UC-MSCs once, and nasal drop 0.5 ml/day (growth medium) for 30 days.
Secretomes
Treatment with tablet (placebo) once for 30 days, IV placebo (NaCl 0.9%) once, and nasal drop 0.5 ml/day (Secretomes) for 30 days.
UC-MSCs and Secretomes
Treatment with tablet (placebo) once for 30 days, IV 0.3 million kg/bb UC-MSCs once, and nasal drop 0.5 ml/day (Secretomes) for 30 days.
Control
Treatment with Metformin once for 30 days, IV placebo (NaCl 0.9%) once, and nasal drop 0.5 ml/day (growth medium) for 30 days.

Locations

Country Name City State
Indonesia PT Prodia StemCell Indonesia Jakarta

Sponsors (1)

Lead Sponsor Collaborator
PT. Prodia Stem Cell Indonesia

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood serum sample Sampling of the subject's blood serum will be carried out during the follicular phase on day 10-12. Follicular phase on day 10-12
Primary Free Androgen index (FAI) Free Androgen index (FAI) is calculated by total testosterone x100/SHBG Follicular phase on day 10-12
Primary Insulin, Glucose Plasma, and Insulin Resistance insulin resistance is calculated by the method: HOMA: HOMA-IR = (insulin x glucose) / 22.5 and HOMA-ß = (20 x insulin) / glucose - 3.5. Follicular phase on day 10-12
Primary Sex Hormone Binding Globulin (SHBG) and Anti-Mullerian Hormone (AMH) Parameter in testing the cytokine/adipokine/hormone profile Follicular phase on day 10-12, and 1,3,6 months after stem cells
Primary Leptin and Adiponectine Profile Parameter in testing the cytokine/adipokine/hormone profile 1,3,6 months after stem cells
Primary TNFa, IL-1 ß, IL-6, IL-10 Profile Parameter in testing the cytokine/adipokine/hormone profile 1,3,6 months after stem cells
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