Melatonin supplementation effect on the Induction of labour rates in first-time MothErs:The MyTIME Trial

Phase 3

Recruiting

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

• Registration Number: ACTRN12623000502639
• Lead Sponsor: Curtin University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-05-17
• Last Update Posted: 11 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 530

Inclusion Criteria

Nulliparous women aged 16 years and over, with a singleton pregnancy in cephalic presentation, without clinical indication for induction, awaiting spontaneous onset of labour, not planning a scheduled birth before 41 weeks unless indicated and able to provide written informed consent to participate in the clinical trial.

Exclusion Criteria

Women with indications for induction of labour or caesarean section prior to 41 weeks because of medical complications; any fetal congenital abnormality or known fetal compromise that would necessitate admission to NICU after birth; any known sensitivity or adverse reaction to melatonin.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Induction of labour extracted from mandatory notification system/ perinatal database. [ At any time post-enrolment]