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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01145144
Other study ID # mmc07204-2006ctil
Secondary ID
Status Completed
Phase N/A
First received May 3, 2010
Last updated June 15, 2010
Start date January 2008
Est. completion date July 2009

Study information

Verified date June 2010
Source Meir Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Interventional

Clinical Trial Summary

The aim of this study was to evaluate the effect of dehydroepiandrosterone supplementation on in vitro fertilization performance and outcome among poor-responder patient.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 42 Years
Eligibility Inclusion Criteria:

- previous poor response to ovarian stimulation in IVF.

Exclusion Criteria:

- patients over the age of 42

- patients who received DHEA at any time.

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
dehydroepiandrosterone crystalline fine powder


Locations

Country Name City State
Israel Meir Medical center IVF unit kfar Saba
Israel Meir Medical Center Kfar Sava

Sponsors (1)

Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary peak estradiol level. No
Primary number of retrieved oocytes. Yes
Primary Embryos that were graded as a top quality (according to the number of cells and percent of fragmentation) Yes
Primary number of embryos reserved for transfer. Yes
Secondary pregnancy rate. Yes
Secondary live birth rate. Yes
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