Mifepristone and Misoprostol for the Termination of Pregnancy up to 70 Days Gestation

Completed

Conditions studied: Medical; Abortion, Fetus

In brief

The purpose of this study is to determine the efficacy and acceptability of a regimen of 200 mg mifepristone (Zacafemyl), followed 24-48 hours later by 800 mcg of buccal misoprostol.

Key facts

Study ID

NCT01966874

Run by

Gynuity Health Projects

People needed

1001

Starts

2011-08-01

Expected to finish

2012-05-01

Last updated by the study team

2013-10-22

Who can join

Age: any. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women of reproductive age
• Gestational age less than or equal to 70 days LMP
• Willing and capable of accepting and participating
• Eligible for medical abortion according to the clinic's evaluation
• Willing to undergo a surgical intervention to complete the abortion if necessary
• Willing to provide an address and/or telephone number for follow up
• Have easy, straightforward access to a telephone and emergency transport

You may not qualify if…

• Gestational age is greater than 70 days LMP
• Suspicion or diagnosis of ectopic pregnancy or undiagnosed adnexal mass
• Use of IUD (note: the woman will be eligible when she removes the IUD)
• Chronic renal failure
• Current long term treatment with corticosteroids
• Allergy to mifepristone, misoprostol, or other prostaglandin
• Coagulopathies or current treatment with anti-coagulants
• Hereditary porphyrias

Where it is running

• Gynuity Health Projects — New York, New York, United States

Full record on ClinicalTrials.gov

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