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Clinical Trial Summary

This study seeks to evaluate the efficacy, side effect profile and acceptability of a medical abortion regimen with mifepristone and two doses of 800 mcg misoprostol buccally at 71-77 and 78-84 days of gestation to further expand the evidence base for the most effective regimens in the late first trimester of pregnancy.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05119439
Study type Interventional
Source Gynuity Health Projects
Contact Ilana G Dzuba, MHS
Phone +1.212.448.1230
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date January 2022
Completion date June 2023

See also
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Completed NCT02343913 - Simplifying Menstrual Regulation (MR): Post Abortion Care in Pakistan N/A
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Recruiting NCT00920465 - Treatment Regimens for Mifegyne and Cytotec Phase 3
Completed NCT00997347 - The Extended Gestational Age Medical Abortion Study Phase 4
Completed NCT03014193 - Simplifying First Trimester Medical Abortion Follow-up N/A
Completed NCT04181541 - Midlevel Versus Physician-provided Medical Abortion in the Second Trimester N/A
Not yet recruiting NCT04905251 - Effectiveness and Safety of Combination Mifepristone/Misoprostol for Medical Abortion
Completed NCT02314754 - Outpatient Medical Abortion With Mifepristone and Misoprostol Through 77 Days of Gestation Phase 4