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Clinical Trial Summary

The aim of this work is to compare the effectiveness of sublingual misoprostol 400 mcg versus 800 mcg for medical treatment of the first trimester missed miscarriage.


Clinical Trial Description

the study will be made on female patients with the first trimester missed abortion confirmed by ultrasound. Participants will be divided into 2 groups one group (A) will receive sublingual Misoprostol 400 mcg and the other group(B) will receive sublingual Misoprostol 800 mcg every 4 hours in both groups up to 3 doses the aim of the study is to compare the efficacy of sublingual Misoprostol in complete termination of the first trimester missed abortion and which route is the best will less side effects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05103098
Study type Interventional
Source Aswan University Hospital
Contact
Status Not yet recruiting
Phase N/A
Start date November 1, 2021
Completion date March 31, 2023

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