Overview

The Effect of a Higher Dose of Dehydroepiandrosterone (DHEA) Supplementation in Poor Responders

Status:
Unknown status
Trial end date:
2016-12-01
Target enrollment:
0
Participant gender:
Female
Summary
The supplementation of Dehydroepiandrosterone (DHEA) has been used in some centers for patients with previous poor ovarian reserve and response in an attempt to improve pregnancy outcomes. However, there still has controversy on the clinical effect on the 75mg/d for the use,especially in Asian people. Whether the double dosage of DHEA in patients with poor ovarian reserve and response in China can improve the IVF outcome with little side effect is unknown. The aim of this randomized controlled study is to compare the effect of a higher dose (150mg daily) and a standard dose (75mg daily) of DHEA on the number of oocytes obtained in poor ovarian responders. The effect of DHEA action on the cumulus cells will be examined.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
ShangHai Ji Ai Genetics & IVF Institute
Treatments:
Dehydroepiandrosterone
Criteria
Inclusion Criteria:

1. age<45 years,

2. subfertility >1 year, and

3. A previous POR (≤3 oocytes with a conventional stimulation protocol of at least 150 IU
FSH per day); or

4. An abnormal ovarian reserve test (i.e. AFC ≤5-7 follicles or AMH ≤0.5-1.1 ng/ml).

Exclusion Criteria:

Patients were excluded if they:

1. had a history of ovarian cystectomy or oophorectomy,

2. had received cytotoxic chemotherapy,

3. had received pelvic irradiation, or

4. had a history of taking testosterone or DHEA supplementation