Cervical ripening /Labour induction in postdate nulliparas; Comparative study of vaginal misoprostol versus vaginal misoprostol with rectal hyoscine-butylbromide

Phase 3

Not yet recruiting

• Conditions: Postdate pregnancy

• Registration Number: PACTR202407560838827

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-06-29
• Last Update Posted: 2024-08-19

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 70

Inclusion Criteria

1. Those who will give consent to the study.
2. Nulliparous pregnant women.
3. Postdate pregnancy.
4. Selected for cervical ripening and induction of labour.
5 Singleton pregnancy with vertex presentation.

Exclusion Criteria

1. maternal co-morbidities like hypertension, diabetes Mellitus,
2. Pregnancy complications like antepartum haemorrhage and severe pre-eclampsia
Those allergic to hyoscine
Those contraindicated to receive prostaglandins like asthma and glaucoma
5. Previous caesarian scar
6. Contraindication to vaginal delivery
Malpresentation

Study & Design

• Study Type: Interventional
• Study Design: Not specified