Comparative Study of two drugs to start labour pains in pregnancy

Not Applicable

• Conditions: Health Condition 1: O80- Encounter for full-term uncomplicated delivery

• Registration Number: CTRI/2022/11/047064
• Lead Sponsor: Dr Ranjana Gupta

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 November 2022

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Uncomplicated pregnancy

2.Singleton live pregnancy with cephalic presentation

3.Term pregnancy (37 - 42 weeks)

4.Intra uterine foetal death

5.Gestational hypertension

6.Primigravida less than 35 years

7.uncomplicated multigravida up to three pregnancies

8.Intact membranes during the time of induction

9.No contraindications for prostaglandins or mifepristone.

Exclusion Criteria

1.Premature membrane rupturing

2.Malpresentations

3.Cephalopelvic disproportion

4.Bad obstetric history or history of previous abortions

5.Previous history of caesarean section or any uterine surgery

6.Multiple pregnancy

7.Placental complications like abruption or placenta praevia

8.Abnormal pattern of foetal heartbeat

9.Parity > 4

10.Active herpes infection

11.Contra indication for prostaglandins

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
â?¢To evaluate the efficacy of oral mifepristone versus misoprostol for pre-induction cervical ripening and term induction of labour.Timepoint: 24 hrs

Secondary Outcome Measures

Name	Time	Method
illTimepoint: nill