Chart Review Study of Medical Abortion

Completed

Conditions studied: Abortion, Medical

In brief

The primary objective of this study is to document the rates of success and serious complications among women having outpatient medical abortions with 200 mg mifepristone + 800 buccal misoprostol at 64-70 days of gestation.

Key facts

Study ID

NCT02841072

Run by

Gynuity Health Projects

People needed

579

Starts

2015-05-01

Expected to finish

2016-04-01

Last updated by the study team

2016-07-21

Who can join

Age: any. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women at 64-70 days of gestation
• Received 200 mg mifepristone + 800 mcg buccal misoprostol for a medical abortion

You may not qualify if…

• Does not meet the inclusion criteria

Where it is running

• Family Planning Associates- Northwest Chicago — Chicago, Illinois, United States
• Family Planning Associates- Downtown Chicago — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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