Intraovarian PRP & Gh in poor ovarian responder

Phase 2

Recruiting

• Conditions: Female infertility of other origin.; Female infertility of other origin; N97.8

• Registration Number: IRCT20091012002576N32
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Age 20-40 years old with abnormal ovarian reserve test.
Antral follicle count<5.
At least one previous IVF cycle <3oocyte was retrieved.

Exclusion Criteria

Ovarian insufficiency due to gonadal dysgenesia and abnormality of chromosoms
Male infertility

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Chemical pregnancy. Timepoint: Two weeks after fetal transfer. Method of measurement: Beta HCG test.;AMH. Timepoint: before and 3 months after intervention. Method of measurement: Measurements blood levels of AMH by Eliza method.

Secondary Outcome Measures

Name	Time	Method
Clinical pregnancy. Timepoint: Four weeks after embryo transfer. Method of measurement: Heart beat activity in transvaginal sonogram.