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RecruitingNCT06564064

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

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Sohag University · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

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

Detailed description

The effect of abdominal binders on patient's wellbeing after cesarean delivery 12 hours and one week after cesarean section

Conditions

Interventions

TypeNameDescription
DEVICEabdominal binderstudy 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

Timeline

Start date
2024-07-15
Primary completion
2024-10-01
Completion
2024-10-15
First posted
2024-08-21
Last updated
2024-08-21

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06564064. Inclusion in this directory is not an endorsement.

The Effect of Abdominal Binders on Patient's Wellbeing After Cesarean Delivery (NCT06564064) · Clinical Trials Directory