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

S

Sohag University

Status

Enrolling

Conditions

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

Treatments

Device: abdominal binder

Study type

Interventional

Funder types

Other

Identifiers

NCT06564064
Soh-Med-24-07-20MS

Details and patient eligibility

About

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

Full description

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

Enrollment

50 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

any female post cesarean section of singleton 34 wks gestaion fetus with previous cs

Exclusion criteria

primary cs any hypertensive disorder with pregnancy any neurologiacal disease general anasthesia or vertical incision

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups, including a placebo group

study group Study group(Group1)
Active Comparator group
Description:
25 participant will be in study group (abdominal binders)
Treatment:
Device: abdominal binder
Control group (Group 2)
Placebo Comparator group
Description:
25 participants will be in control group
Treatment:
Device: abdominal binder

Trial contacts and locations

1

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Central trial contact

abdou s aitallah, professor; esraa s abd ellatif, resident

Data sourced from clinicaltrials.gov

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