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Outpatient Induction of Labour Using Intracervical Foley Catheter

NCT05622968 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 88

Last updated 2025-01-17

No results posted yet for this study

Summary

Prospective quasi-experimental study between a study population who will receive outpatient induction of labour using intracervical Foley catheter, followed by the inpatient induction using intravaginal prostaglandin and a control group of women with similar characteristics undergoing inpatient labour induction with intravaginal prostaglandin (standard management)

Conditions

  • Pregnancy Related
  • Induction of Labor Affected Fetus / Newborn

Interventions

DEVICE

Foley catheter

Insertion of 18G Foley catheter into the cervical canal and inflating the balloon to 60 mls using sterile water

DRUG

Intravaginal prostaglandin E2

Insertion of intravaginal Dinoprostone

Sponsors & Collaborators

  • Hospital Kemaman

    lead OTHER

Principal Investigators

  • Zahar Zakaria, MD · Hospital Kemaman

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2024-09-01
Completion
2024-09-01

Countries

  • Malaysia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05622968 on ClinicalTrials.gov