Propranolol and Misoprostol Versus Misoprostol Alone for Induction of Labor in Primigravidas

Induction of Labor Affected Fetus / Newborn Clinical Trial

Official title: Propranolol and Misoprostol Versus Misoprostol Alone for Induction of Labor In Primigravidas

Status Completed

Clinical Trial Summary

To compare propranolol and misoprostol versus misoprostol alone for induction of labour in primigravidas

Clinical Trial Description

Candidates will be randomized into 2 groups according to a computer generated sequence. Each candidate will be assigned an opaque sealed envelope containing a paper with her group on it. Both the patient and doctor on duty will be blinded to which group the patient was assigned to.

• Study procedure:

1. Written informed consent will be obtained from all participants prior to the study.

2. Full history taking.

3. General examination.

Patients will be subjected to the following:

• Patients attending labour room for induction of labour will be divided into two groups.

• Both groups, women are induced with Tab misoprostol 25μg applied to posterior vaginal fornix under aseptic precaution and every 6 hours for a maximum of 4 doses.

• In group 1, after induction is started with misoprostol placement, 30 minutes will pass before administration of oral Propanolol 20mg

• In group 2, after induction is started with misoprostol placement, 30 minutes will pass before administration of oral placebo in the form of sugary tablets.

• After induction, women will be monitored for fetal and maternal wellbeing and progress of labour. ;

Related Conditions & MeSH terms

• Induction of Labor Affected Fetus / Newborn

• NCT number: NCT04533841
• Study type: Interventional
• Source: Ain Shams University
• Status: Completed
• Phase: Phase 2
• Start date: February 1, 2020
• Completion date: September 15, 2020