a Predictive Scheme for Poor Responders in IVF Cycles

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

928 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-01-31

Study Completion Date

2013-12-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Infertility

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Group I

poor responder females with age less than 35

transvaginal Ultrasound

Intervention Type OTHER

Group II

poor responder females with age more than 35

transvaginal Ultrasound

Intervention Type OTHER

Interventions

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transvaginal Ultrasound

Intervention Type OTHER

Eligibility Criteria

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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.

Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No