RecruitingNot ApplicableNCT06564064

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

The Effect of Abdominal Binders on Patient's Wellbeing After Cesarean Delivery :a Prospective Comparative Study

Sponsor

Sohag University

Enrollment

50 participants

Start Date

Jul 15, 2024

Study Type

INTERVENTIONAL

Conditions

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

Summary

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

Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called abdominal binder for people with effect of abdominal binders on patient ( pain, quality of recovery ) after cesaean section. The study is currently recruiting participants at 1 location. People eligible for this study include women.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEabdominal 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

Locations(1)

Sohag university Hospital

Sohag, Egypt

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NCT06564064