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The REDUCED Trial: REDucing the Utilization of CEsarean Sections for Dystocia

NCT02874443 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 88918

Last updated 2025-12-15

No results posted yet for this study

Summary

This project is a clustered randomized controlled trial of a knowledge translation intervention of new ACOG guidelines for the diagnosis of poor progress in labor. The intent is to reduce the rate of cesarean section (CS) in first time mothers at term (\>= 37 weeks), with a vertex presenting singleton fetus, without increasing maternal or neonatal morbidity. The guidelines were developed from data from the Consortium for Safe Labor. The unit of randomization will be sites in Alberta that deliver

Conditions

  • Cesarean Section, Dystocia

Interventions

OTHER

Knowledge Translation of labor management guidelines

Sponsors & Collaborators

  • University of Calgary

    lead OTHER

Principal Investigators

  • Stephen Wood, MD MSc · University of Calgary

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-31
Primary Completion
2020-02-28
Completion
2020-03-30

Countries

  • Canada

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 NCT02874443 on ClinicalTrials.gov