Induction of Abortion in the Second Trimester

Status Completed

Clinical Trial Summary

To compare between the effects of misoprostol with hyoscine N-butyl bromide and misoprostol alone on shortening the time of abortion induction in the second trimester.

Clinical Trial Description

The study will be conducted on 40 women who will undergo induction of abortion between 13-24 weeks with positive fetal pulsation. They will be randomly assigned to receive either only misoprostol 400 μg under the generic name of misotac tablets produced by Sigma company according to FIGO classification 2019 and a halved dose if the patient has a history of one or two cesarean sections, or misoprostol 400 μg plus intramuscular administration of hyoscine N-butyl bromide under the generic name of buscopan ampoule produced by Sanofi company. ;

Study Design

Related Conditions & MeSH terms

Abortion, Second Trimester

Clinical Trial Details

NCT number	NCT06207539
Study type	Interventional
Source	Ain Shams Maternity Hospital
Contact
Status	Completed
Phase	Early Phase 1
Start date	December 1, 2022
Completion date	April 30, 2023

View Details

See also
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Completed	`NCT00495560` - A Pilot Study of Priming Before Induction Termination of Pregnancy	N/A
Completed	`NCT05099991` - Transcervical Balloon Compared to Osmotic Dilators Prior to Surgical Abortion	N/A