Dehydroepiandrosterone Supplementation for Poor Responder Patients During in Vitro Fertilization Treatment

Sponsor
Meir Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT01145144
Collaborator
(none)
2
2
18

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Drug: dehydroepiandrosterone crystalline fine powder
N/A

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Study Start Date :
Jan 1, 2008
Actual Primary Completion Date :
Jul 1, 2009
Actual Study Completion Date :
Jul 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: DHEA supplementation

DHEA was added to induction of ovulation by recombinant FSH and recombinant LH, in IVF long protocol

Drug: dehydroepiandrosterone crystalline fine powder

No Intervention: only induction of ovulation by same long protocol without DHEA

Outcome Measures

Primary Outcome Measures

  1. peak estradiol level. []

  2. number of retrieved oocytes. []

  3. Embryos that were graded as a top quality (according to the number of cells and percent of fragmentation) []

  4. number of embryos reserved for transfer. []

Secondary Outcome Measures

  1. pregnancy rate. []

  2. live birth rate. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 42 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Meir Medical center IVF unit kfar Saba Israel
2 Meir Medical Center Kfar Sava Israel

Sponsors and Collaborators

  • Meir Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01145144
Other Study ID Numbers:
  • mmc07204-2006ctil
First Posted:
Jun 16, 2010
Last Update Posted:
Jun 16, 2010
Last Verified:
Jun 1, 2010

Study Results

No Results Posted as of Jun 16, 2010