A Prospective Randomized Trial Comparing Qam With Qpm Daily Dosing in Assisted Reproductive Technologies

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City:		Reston
State:		Virginia
Zip Code:		20190

Conditions:		Infertility
Purpose:		This is a prospective randomized trial comparing the outcome in women undergoing IVF/ICSI when taking their gonadotropin dosage in the morning (am) or evening (pm).
Study Summary:
Criteria:		Inclusion Criteria: - women between 21-42 undergoing IVF Exclusion Criteria: - women > 45, - women with one ovary, - donor egg, - surrogacy, - FET cycles, - uterine problems, - large fibroids
NCT ID:		NCT01139593
Primary Contact:		Fady Sharara, M.D Phone: 7034377722 Email: fsharara@vcrmed.com
Backup Contact:		N/A
Location Contact:		Reston, Virginia 20190 United States Fady Sharara, M.D Phone: 703-437-7722 Email: info@vcrmed.com Site Status: Recruiting

Data Source:		ClinicalTrials.gov
Date Processed:		May 19, 2013
Modifications to this listing:		Only selected fields are shown, please use the link below to view all information about this clinical trial.
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