Different methods for trying normal delivery

Phase 4

Not yet recruiting

• Conditions: Encounter for full-term uncomplicated delivery, (2) ICD-10 Condition: O618||Other failed induction of labor,

• Registration Number: CTRI/2022/04/042218
• Lead Sponsor: GIMS Gadag

Brief Summary

Induction of labour involves the artificial stimulation of uterine contractions with the aim to achieve safe vaginal delivery and performed approximately 15 percentage of all pregnancy. Induction of labour has two components. Cervical ripening and stimulation of uterus to achieve dilatation of cervix and delivery of fetus .

Decision   of induction of labour is taken for the benefits are more than risks of continuation of pregnancy.

Foley catheter induction. acts by exerting pressure into cervical canal and seperates decidua and stimulate the local release of prostaglandins. Foley catheter is most commonly used in current clinical practice. There is reduced risk of hyperstimulation and fetal distress with Foley catheter induction of labour.

Pharmacological methods being used are prostaglandins like Dinoprostone and Misoprostol.

Presently misoprostol gain the popularity due to the advantages like low cost stability of drug at room temperature, easy handling, storage, easy administration and good efficiency .

 The purpose of this study is to compare the safety and success of pervaginal misoprostol, intracervical dinoprostone, intracervical Foley catheter for induction of labour.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2022-04-22
• Study Start: 2022-04-28

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 273

Inclusion Criteria

Patient with 1.singleton, 2.cephalic, 3.term gestation, 4.intact membranes, 5.live fetus, 6.absence of uterine contractions, 7.Informed written consent.

Exclusion Criteria

1.Pregnancy induced hypertension, 2.fetal distress, 3.previous cesarian section, 4.uterine surgery, 5.intrauterine growth reduction , 6.malpresentation , 7.oligohydramnios, 8.polyhydramnios 9.diabetic mellitus.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
rate of vaginal delivery	24 hours after induction

Secondary Outcome Measures

Name	Time	Method
Rate of cesarean section

Trial Locations

Locations (1)

Gadag Institute of Medical Sciences, Gadag; 🇮🇳 Gadag, KARNATAKA, India

Gadag Institute of Medical Sciences, Gadag

🇮🇳Gadag, KARNATAKA, India

Hanumant v nipanal

Principal investigator

9448001054

hanumantvn.1210@gmail.com