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
Summary
The effect of abdominal binders on patient's wellbeing after cesarean delivery
Eligibility
Sex: FEMALE
Inclusion Criteria1
- any female post cesarean section of singleton 34 wks gestaion fetus with previous cs
Exclusion Criteria1
- primary cs any hypertensive disorder with pregnancy any neurologiacal disease general anasthesia or vertical incision
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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)
View Full Details on ClinicalTrials.gov
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NCT06564064