Once Daily vs Twice Daily Administration of Gonadotropins in Assisted Reproductive Technologies (ART)
NCT ID: NCT00740025
Last Updated: 2010-10-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
200 participants
OBSERVATIONAL
2006-01-31
2010-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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QD
Women who received their meds as QD administration
No interventions assigned to this group
BID
Women who received their gonadotropins as a BID dose
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* endometriomas
* severe cervical stenosis
* testicular sperm
21 Years
39 Years
FEMALE
No
Sponsors
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Virginia Center for Reproductive Medicine
OTHER
Responsible Party
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Virginia Center for Reproductive Medicine
Principal Investigators
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Fady I Sharara, M.D
Role: PRINCIPAL_INVESTIGATOR
Virginia Center for Reproductive Medicine
Locations
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Virginia Center for Reproductive Medicine
Reston, Virginia, United States
Countries
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Other Identifiers
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1-Sharara
Identifier Type: -
Identifier Source: org_study_id