MedTrace Logo

The Use of Abdominal Binders in Patients Undergoing Cesarean Sections

NCT02129894 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 210

Last updated 2014-05-02

No results posted yet for this study

Summary

To see if the use of Abdominal Binders improves patients out comes after cesarean delivery

Conditions

  • Cesarean Section Post Operative Management

Interventions

DEVICE

abdominal Binder

placement of abdominal binder

Sponsors & Collaborators

  • St. Luke's Hospital, Pennsylvania

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2014-09-30
Completion
2014-10-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT02129894 on ClinicalTrials.gov