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The Effect of Abdominal Binders on Patient's Wellbeing After Cesarean Delivery

NCT06564064 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-08-21

No results posted yet for this study

Summary

The effect of abdominal binders on patient's wellbeing after cesarean delivery

Conditions

  • Effect of Abdominal Binders on Patient ( Pain, Quality of Recovery ) After Cesaean Section

Interventions

DEVICE

abdominal binder

study group will be abdominal binders and control group will be control group , 12 hrs and one week later VAS and QOR 40 will assess patient,s wellbeing

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-07-15
Primary Completion
2024-10-01
Completion
2024-10-15

Countries

  • Egypt

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 NCT06564064 on ClinicalTrials.gov