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This study is being conducted to evaluate the impact of a 91-day extended cycle oral contraceptive compared to two 28-day oral contraceptive regimens on hemostatic parameters in healthy women.
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Lead Sponsor
Teva Women's Health
NCT06664788 · Hemostasis, Hemostatic Techniques
NCT07466719 · Obstetric Hemostasis, Intravascular Hemolysis, and more
NCT07349251 · Premature Infant, Hemostasis
NCT07258576 · Female Sex Hormones, Menstrual Cycle, and more
NCT06679491 · Menstrual Cycle, Resistance Training, and more
Teva Investigational Site
San Diego, California
Teva Investigational Site
San Diego, California
Teva Investigational Site
San Diego, California
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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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