Effects of intraovarian PRP, rFSH injection in poor ovarian responder

Phase 2

Recruiting

• Conditions: Infertility.; N97.8; Female inf

• Registration Number: IRCT20091012002576N33
• 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: 30

Inclusion Criteria

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
FSH,LH,AMH,Esteradiol levels. Timepoint: Before and three months after intervention. Method of measurement: Laboratory tests.;Chemical pregnancy. Timepoint: Two weeks after embryo transfer. Method of measurement: Bhcg tests.;Number of MII oocyte. Timepoint: Three months after intervention. Method of measurement: Embryologist report.

Secondary Outcome Measures

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