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Clinical Trial Summary

Efficacy of sublingual versus vaginal misoprostol in termination of first trimester missed abortion


Clinical Trial Description

study will be made on female patients with first trimester missed abortion confirmed by ultrasound . Participants will be divided into 2 groups one group (A) will receive sublingual Misoprostol and the other group(B) will receive vaginal Misoprostol as a 800 micro grams every 4 hours in both groups up to five doses the aim of the study is to compare efficay of sublingual and vaginal Misoprostol in complete termination of first trimester missed abortion and which route is the best will less side effects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05001061
Study type Interventional
Source Cairo University
Contact Ahmed Emam
Phone 01003304781
Email emam3882@gmail.com
Status Not yet recruiting
Phase Early Phase 1
Start date August 3, 2021
Completion date October 16, 2021

See also
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