Actively Recruiting

Phase Not Applicable
FEMALE
Healthy Volunteers
NCT06564064

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

Led by Sohag University · Updated on 2024-08-21

50

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patients post cesarean section with singleton fetus at 34 weeks gestation or later
  • Previous cesarean section history
Not Eligible

You will not qualify if you...

  • Primary cesarean section
  • Any hypertensive disorder during pregnancy
  • Any neurological disease
  • Use of general anesthesia
  • Vertical incision during cesarean section

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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2
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Trial Site Locations

Total: 1 location

1

Sohag university Hospital

Sohag, Egypt, Sohag

Actively Recruiting

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Research Team

E

esraa s abd ellatif, resident

CONTACT

A

abdou s aitallah, professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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