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Clinical Trials/NCT02351193
NCT02351193CompletedNot Applicable

A Predictive Scheme to Assess the Outcome of IVF/ICSI Cycles in Poor Responders. an Observational Study in Egypt

Dina Mohamed Refaat Dakhly1 site in 1 country928 target enrollmentStarted: January 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
928
Locations
1
Primary Endpoint
Number of MII oocytes

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
20 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

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.

Outcomes

Primary Outcomes

Number of MII oocytes

Time Frame: 2 years

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Dina Mohamed Refaat Dakhly
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Dina Mohamed Refaat Dakhly

Lecturer of Obstetrics and Gynecology

Woman's Health University Hospital, Egypt

Study Sites (1)

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