Clinical Trial: Treatment of Incomplete Abortion With 600 Mcg Oral Misoprostol Compared to Standard Surgical Treatment
Study Status: Completed
Recruit Status: Completed
Study Type: Interventional
Official Title: Misoprostol for Treatment of Incomplete Abortion
Brief Summary: This study aims to compare the efficacy, side effects profile and acceptability of a single dose of 600mcg misoprostol taken orally compared to standard surgical treatment as per local protocols for the treatment of incomplete abortion.
Detailed Summary:
Sponsor: Gynuity Health Projects
Current Primary Outcome: complete resolution of signs/symptoms of incomplete abortion without recourse to surgery at any point for any reason [ Time Frame: one week after initial treatment ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- side effects [ Time Frame: measured at follow up visit one week after initial treatment ]
- acceptability [ Time Frame: measured at follow up visit one week after initial treatment ]
Original Secondary Outcome: Same as current
Information By: Gynuity Health Projects
Dates:
Date Received: April 28, 2008
Date Started: May 2006
Date Completion:
Last Updated: May 5, 2008
Last Verified: May 2008
