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Longitudinal Hemostatic Profile After Stopping Estroprogestative Contraceptives — PILL-OFF  

Contraception Clinical Trial

Official title:
Longitudinal Hemostatic Profile After Stopping Estroprogestative Contraceptives: a Prospective Cohort Study

Clinical Trial Summary

This prospective cohort evaluates the longitudinal profile of hemostatic biomarkers during the first 3 months after having stopped a combined oral contraceptive.

Clinical Trial Description

Women using a combined oral contraceptive (COC) and who have decided to stop it or switch it to a non-estrogenic contraceptive are included. At baseline, before the COC is stopped, and at multiple time points during the 3 months of follow-up, blood will be drawn to evaluate the hemostatic profile. Findings are compared with a control group of women without an estrogenic contraceptive, who are also followed for 3 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03949985
Study type Observational
Source University Hospital, Geneva
Contact
Status Completed
Phase
Start date October 8, 2018
Completion date September 14, 2020
View Details
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