Clinical Trials Directory

Trials / Completed

CompletedNCT02132559

Effect of Dehydroepiandrosterone Administration in Patients With Poor Ovarian Response According to the Bologna Criteria

Status
Completed
Phase
Study type
Observational
Enrollment
386 (actual)
Sponsor
Chinese Medical Association · Network
Sex
Female
Age
23 Years – 45 Years
Healthy volunteers
Accepted

Summary

Women with low ovarian reserve typically respond less well to the drugs used to stimulate the ovary during IVF treatment and produce fewer eggs and, as a result, are less likely to fall pregnant either naturally or after fertility treatment. The ideal stimulation regimen for poor responders is currently unknown. Dehydroepiandrosterone (DHEA) has been reported to improve pregnancy chances for poor responders, and is now utilized by approximately one third of all IVF centers world-wide. However, the current clinical evidence for DHEA on improvement of ovarian response and IVF outcome is insufficient. The validity of the results of the former studies, especially the varied inclusion criteria used to specify poor responders, is a subject of debate. Recently a uniform definition on poor ovarian response, the Bologna criteria, has been proposed by the European Society for Human Reproduction and Embryology(ESHRE). However, no studies have been performed study to evaluate the potential effects of DHEA supplementation according to these standards. The purpose of this study is to assess the impact of DHEA supplementation on IVF outcome of poor ovarian responders that fulfill the Bologna criteria.

Conditions

Interventions

TypeNameDescription
DRUGDHEA

Timeline

Start date
2011-10-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2014-05-07
Last updated
2014-05-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02132559. Inclusion in this directory is not an endorsement.