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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00674232
Study type Interventional
Source Gynuity Health Projects
Contact
Status Completed
Phase N/A
Start date May 2006
Completion date October 2007

See also
  Status Clinical Trial Phase
Completed NCT01939457 - 400mcg Sublingual Misoprostol as First Line Treatment N/A
Recruiting NCT05342467 - Gemeprost Versus Dinoprostone in First Trimester Miscarriages Phase 2
Completed NCT02707653 - Sublingual Misoprostol for the Treatment of Incomplete Abortion: Operations Research N/A
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
Completed NCT01539408 - Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion in Nigeria Phase 1
Completed NCT03622073 - Misoprostol Treatment of Mid Trimester Incomplete Abortion by Midwives and Doctors in Uganda. N/A
Completed NCT01743508 - Misoprostol Treatment of Incomplete Abortion by Midwives and Physicians in Uganda N/A