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Clinical Trial Summary

This pilot study seeks to evaluate the safety, acceptability and feasibility of a shortened outpatient procedure for medical abortion at 13-18 weeks gestation. It also seeks to document the roles of health workers in providing services related to later abortion care. Participants will take a single dose of 200 mg mifepristone orally, followed 24-48 hours later with 400 mcg misoprostol sublingually prior to arriving at the study clinic. Repeat doses of 400 mcg misoprostol will be administered sublingually every three hours at the clinic until the abortion is achieved. If expulsion does not occur by a certain time prior to the clinic closing that day, D&E will be performed to complete the abortion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04063904
Study type Interventional
Source Gynuity Health Projects
Contact
Status Terminated
Phase Phase 4
Start date October 16, 2019
Completion date April 3, 2021

See also
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