Clinical trial to study different methods of induction agents to induce labour

Comparison of efficacy of different modes of induction in predicting the outcome of labour- A Randomized controlled trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/06/019614

Enrollment

300

Registered

2019-06-11

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Active Control group Prostaglandin E2 gel: Prostaglandin E2 gel 0.5mg vaginally maximum 3doses 6hrs apart Control Intervention1: Active Control group Oral Misoprostol: Misoprostol 25mc

Eligibility

Inclusion criteria

Inclusion criteria: GA more than 37weeks,irrespective of parity Singleton,cephalic Intact membranes Unfavourable cervix Reassuring Cardiotocography

Exclusion criteria

Exclusion criteria: Fetal malpresentation Rupture of membranes Multifetal gestation Non reassuring FHR changes Fetal growth restriction Fetal demise Prev LSCS or any uterine surgery Anomalous fetus

Design outcomes

Primary

Measure	Time frame
1.Time interval between induction and active phase of labour, 2.Time interval between induction and delivery 3.Patients who had vaginal delivery within 24hours from inductionTimepoint: Time of induction to 72hours maximum	—

Secondary

Measure	Time frame
1.Mode of delivery, 2.Maternal complications, 3.Fetal outcomesTimepoint: Intrapartum to 48hrs from delivery	—

Countries

India

Contacts

Public ContactDr Kurian Joseph

Joseph nursing home

drkurian@gmail.com9840599969

Outcome results