a Predictive Scheme for Poor Responders in IVF Cycles

Completed

• Conditions: Infertility
• Interventions: Other: transvaginal Ultrasound

• Registration Number: NCT02351193
• Lead Sponsor: Dina Mohamed Refaat Dakhly

Brief Summary

While practicing the different assisted reproductive techniques, the investigators are faced daily by the problem of poor responder females, and the debate about predicting its results based on the outcome of the different ORTs used. Due to the cost of AMH as an indicator for ovarian response, the need to re-assess its role was essential in our community, which led us to conduct this prospective multi-center IVF study.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-01
• Primary Completion: 2013-12
• Study Completion: 2013-12
• Status Verified: 2015-01
• Study First Submitted: 2015-01-26
• Study First Submitted QC: 2015-01-29
• Study First Posted: 2015-01-30
• Last Update Submitted: 2015-01-30
• Last Update Posted: 2015-02-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 928

Inclusion Criteria

• normal body mass index (BMI)
• AMH from 0.5-1.1 ng/ml.
• previous history of ≤3 oocytes retrieved using conventional long stimulation protocol

Exclusion Criteria

• Females suffering from other causes of infertility as tubal, uterine factors or known cases of endometriosis
• severe cases of male factor as azospermia
• females who were unable or not willing to participate in the study were excluded from the study.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Group I	transvaginal Ultrasound	poor responder females with age less than 35
Group II	transvaginal Ultrasound	poor responder females with age more than 35

Primary Outcome Measures

Name	Time	Method
Number of MII oocytes	2 years

Trial Locations

Locations (1)

Kasr el aini hospital; 🇪🇬 Cairo, Egypt