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Two Mifepristone Doses and Two Intervals of Misoprostol Administration for Termination of Early Pregnancy : A Randomised Factorial Controlled Equivalence Trial

OBJECTIVE: To compare the efficacy of 100 mg and 200 mg of mifepristone and 24- and 48-hour intervals to administration of 800 microg vaginal misoprostol for termination of early pregnancy. DESIGN: Placebo-controlled, randomized, equivalence trial, stratified by centre. SETTING: 13 departments of ob...

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Bibliographic Details
Main Authors: von Hertzen, H., Piaggio, G., Wojdyla, D., Marions, L., My Huong, N. T., Tang, O. S., Fang, A. H., Wu, S. C., Kalmar, L., Mittal, S., Erdenetungalag, R., Horga, M., Pretnar-Darovec, A., Kapamadzija, A., Dickson, K., Anh, N. D., Tai, N. V., Tuyet, H. T., Peregoudov, A.
Language:EN
Published: 2012
Subjects:
Nonsteroidal Abortifacient Agents
effects
Steroidal Abortifacient Agents
Abortion, Induced
Adult
Drug Administration Schedule
Female
Humans
Mifepristone
Misoprostol
Pregnancy
First Pregnancy Trimester
Tablets
Treatment Outcome
Treatment Refusal
Online Access:http://hdl.handle.net/10986/5141

Internet

http://hdl.handle.net/10986/5141

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