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This is a pilot study to determine the feasibility for a randomized controlled trial of two forms of intrauterine contraception: the Levonorgestrel intrauterine system (LNG-IUS) and the Copper T 380A.
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Lead Sponsor
University of Chicago
Collaborators
NCT06345586 · Contraception
NCT07115849 · Eumenorrhea, Intrauterine Devices, Medicated, and more
NCT06672016 · Female Contraception
NCT07393334 · Male Contraception, Semen Volume, and more
NCT07365904 · Contraception
University of Illinois at Chicago
Chicago, Illinois
University of Chicago
Chicago, Illinois
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Data Source & Attribution
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.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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