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Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion in Nigeria

Incomplete Abortion Clinical Trial

Official title:
Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion

Clinical Trial Summary

Women diagnosed with incomplete abortion in this health facility will be randomized to receive one of the following regimens: 400 mcg sublingual misoprostol in one dose or standard surgical treatment (MVA). The investigators hypothesize that treatment of incomplete abortion with misoprostol using 400 mcg administered sublingually will be as effective as surgical evacuation.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01539408
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase Phase 1
Start date August 2009
Completion date October 2010
View Details
See also
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Not yet recruiting NCT05343546 - Ideal Timing of Intrauterine Contraception Insertion After Medical Management of First Trimester Incomplete Abortion N/A
Recruiting NCT01775917 - The Role of Uterine Artery Doppler Parameters in the Management of Retained Products of Conception. N/A
Completed NCT00466999 - Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion N/A
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Completed NCT01743508 - Misoprostol Treatment of Incomplete Abortion by Midwives and Physicians in Uganda N/A