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This was a Phase I multi-center, randomized study in 40 healthy, sexually active women not at risk for pregnancy due to previous female sterilization. The male partners of the participants were consen...
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Lead Sponsor
CONRAD
NCT06355713 · Implant Complication, Contraceptive Device; Complications
NCT07437235 · Intrauterine Contraceptive Device Complication
NCT07264933 · Scar Niche, Myometrial Remodeling, and more
NCT06000423 · Bleeding, Contraceptive Device; Complications
NCT06550544 · Contraceptive Device; Complications
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania
Eastern Virginia Medical School
Norfolk, Virginia
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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