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Internal Versus External Tocodynamometry and Labor Outcome

NCT02941393 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1500

Last updated 2018-03-20

No results posted yet for this study

Summary

In this study, parturients will be randomized to either internal or external tocodynamometry contractions' follow up. Investigators recruit primiparous, those who try to have vaginal birth after cesarean section and multiparous, who need oxytocin during labor. Primary endpoint is the number of operative labors in each group. Secondary endpoints are the duration of labor, the use of oxytocin and the condition of the newborn.

Conditions

  • Dystocia
  • Contractions

Interventions

DEVICE

Intrauterine pressure catheter

DEVICE

External tocodynamometry

Sponsors & Collaborators

  • Central Finland Hospital District

    collaborator OTHER

  • Tampere University Hospital

    lead OTHER

Principal Investigators

  • Tuija Hautakangas, MD · Central Finland Central Hospital, Tampere University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2017-12-31
Completion
2017-12-31

Countries

  • Finland

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 NCT02941393 on ClinicalTrials.gov