Effect of abdominal binders on recovery after cesarean delivery
The Effect of Abdominal Binders on Patient's Wellbeing After Cesarean Delivery :a Prospective Comparative Study
This study tests whether using abdominal binders can help women recover better and feel less pain after having a cesarean delivery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Sex | Female |
| Sponsor | Sohag University Academic / other |
| Locations | 1 site (Sohag) |
| Trial ID | NCT06564064 on ClinicalTrials.gov |
What this trial studies
This study investigates how abdominal binders impact the wellbeing of women following a cesarean delivery. It focuses on measuring pain levels and quality of recovery at two time points: 12 hours and one week post-surgery. The methodology involves comparing outcomes between patients who use abdominal binders and those who do not. The goal is to determine if these binders can enhance recovery and reduce discomfort after cesarean sections.
Who should consider this trial
Good fit: Ideal candidates are females who have undergone a cesarean section with a singleton fetus at 34 weeks gestation or later and have a history of previous cesarean deliveries.
Not a fit: Patients who had a primary cesarean section, have hypertensive disorders during pregnancy, neurological diseases, or underwent general anesthesia may not benefit from this study.
Why it matters
Potential benefit: If successful, this could lead to improved recovery experiences for women after cesarean deliveries.
How similar studies have performed: There is limited information on similar studies, making this approach relatively novel in assessing the use of abdominal binders post-cesarean delivery.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Sohag
- Sohag university Hospital — Sohag, Egypt (Recruiting)
Study contacts
- Study coordinator: esraa s abd ellatif, resident
- Email: esraa011002@med.sohag.edu.eg
- Phone: 01157145274
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.