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Inpatient and Outpatient Balloon Catheter Cervical Ripening

NCT04342741 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-04-13

No results posted yet for this study

Summary

A randomised controlled trial comparing cervical ripening using foley catheter as in- or outpatient setting.

Conditions

  • Caesarean Section; Infection

Interventions

DEVICE

Foley catheter cervical ripening

Participants were assessed when labour was established or the following morning.

Sponsors & Collaborators

  • National University of Malaysia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-08-01
Primary Completion
2018-05-31
Completion
2018-05-31

Countries

  • Malaysia

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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 NCT04342741 on ClinicalTrials.gov