Investigating the therapeutic effect of PRP (Platelet-Rich Plasma) in ovarian functio

Phase 2

Recruiting

• Conditions: Women with poor response to ovarian stimulation.; Female infertility associated with anovulation; N97.0

• Registration Number: IRCT20181216042006N2
• Lead Sponsor: Birjand University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

Age range from 25 to 45 years
The amount of FSH hormone is higher than 12
The amount of AMH hormone is lower than 1
Poor response to ovulation stimulating drugs in previous cycles
Donor egg candidate

Exclusion Criteria

The presence of any ovarian cyst confirmed by a gynecologist
People with polycystic ovary confirmed by a gynecologist
People with underlying medical diseases (hypertension and diabetes)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
FSH hormone level. Timepoint: A few days before the injection and the first menstrual cycle after the injection. Method of measurement: Measurement in the laboratory.;AMH hormone level. Timepoint: A few days before the injection and the first menstrual cycle after the injection. Method of measurement: Measurement in the laboratory.;LH hormone level. Timepoint: A few days before the injection and the first menstrual cycle after the injection. Method of measurement: Measurement in the laboratory.;AFC number. Timepoint: A few days before the injection and the first menstrual cycle after the injection. Method of measurement: sonography.