Randomized Clinical Trial between Titrated oral dose of Misoprostol and Propess for Induction of Labor

Phase 1

Completed

• Conditions: Induction of labor; Reproductive Health and Childbirth - Childbirth and postnatal care

• Registration Number: ACTRN12611000420943
• Lead Sponsor: King Abdulaziz University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-04-21
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 150

Inclusion Criteria

1.Singleton pregnancy for induction of labor.
2.Consent is taken.
3.No contraindication to use either drugs.
4.Bishop score <6.

Exclusion Criteria

1.<34 wks gestation.
2.Severe PIH (abnormal LFT’s, protein>1g/day, BPgreater than or equal to 160/100).
3.Previous C/S or other uterine surgery.
4.Twins.
5.Para (number of previous deliveries) four.
6.Uterine contractions.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To achieve induction[After delivery and before discharge from the hospital (within five days of randomization).]

Secondary Outcome Measures

Name	Time	Method
ausea, vomitting, and any other side-effects including hypersensitivity reaction. Chart review will be done immediately after delivery will be done.[After deilvery and before discharge from the hospital (within five days).]