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 |
---|---|---|
|
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
- peak estradiol level. []
- number of retrieved oocytes. []
- Embryos that were graded as a top quality (according to the number of cells and percent of fragmentation) []
- number of embryos reserved for transfer. []
Secondary Outcome Measures
- pregnancy rate. []
- 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
Keywords provided by ,
,
Additional relevant MeSH terms: