Clinical Trial: Buccal Versus Vaginal Misoprostol in Surgical Termination of the First Trimester Missed Abortion in Erbil

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: Buccal Versus Vaginal Misoprostol for Cervical Ripening Prior to Surgical Termination of the First Trimester Missed Abortion in Erbil

Brief Summary: The purpose of this study is to determine the effectiveness of buccal misoprostol and comparing this with vaginal route of the same drug.

Detailed Summary:
Sponsor: Hawler Medical University

Current Primary Outcome: To compare the efficacy of buccal administration to the more commonly vaginal route for preoperative cervical and priming in patients with first trimester surgical abortion. (Buccal Vs. Vaginal Misoprostol in the First Trimester Missed Abortion.) [ Time Frame: March 2007 to March 2008 ]

Original Primary Outcome: Same as current

Current Secondary Outcome: The secondary objectives are to compare the side effects and acceptability by the subjects. [ Time Frame: March 2007 to March 2008 ]

Original Secondary Outcome: Same as current

Information By: Hawler Medical University

Dates:
Date Received: May 1, 2009
Date Started: March 2007
Date Completion:
Last Updated: May 1, 2009
Last Verified: May 2009