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Is Routine Cervical Dilatation Necessary During Elective Caesarean Section? A Randomised Controlled Trial

NCT01954719 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2013-10-07

No results posted yet for this study

Summary

The purpose of this prospective randomised study was to determine the effect of routine cervical dilatation during elective caesarean section on maternal morbidity

Conditions

  • Failure of Cervical Dilatation
  • Complications; Cesarean Section
  • Wound Infection,
  • External Causes of Morbidity and Mortality

Interventions

PROCEDURE

cervix dilated after surgery

The surgeon inserted his or her double-gloved index digit in the cervical canal to dilate it and removed the outer gloves after digital dilatation of the cervix.

PROCEDURE

control group

surgeon not dilated cervix after surgery

Sponsors & Collaborators

  • Bakirkoy Dr. Sadi Konuk Research and Training Hospital

    lead OTHER_GOV

Principal Investigators

  • hüseyin cengiz, md · Bakırkoy Dr. Sadi Konuk Training and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
CROSSOVER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-12-31
Completion
2014-01-31

Countries

  • Turkey (Türkiye)

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 NCT01954719 on ClinicalTrials.gov