Actively Recruiting

Phase Not Applicable
Age: 30Years - 45Years
FEMALE
NCT07130747

Effect of Myofascial Release Versus Deep Friction Massage on Abdominal Recovery and Scar After Cesarean Section

Led by Cairo University · Updated on 2025-08-19

36

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study was done to compare the effect of myofascial release versus deep friction massage on abdominal recovery and scar after cesarean section.

CONDITIONS

Official Title

Effect of Myofascial Release Versus Deep Friction Massage on Abdominal Recovery and Scar After Cesarean Section

Who Can Participate

Age: 30Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • All postpartum women more than 6 months postnatal with a post-Cesarean-section scar
  • Postpartum women with a well-healed cesarean section scar causing chronic pain in the scar, pelvis, or abdomen
  • Age between 30 and 45 years
  • Body mass index (BMI) less than 30 kg/m8
Not Eligible

You will not qualify if you...

  • Pregnant women or those planning for pregnancy
  • Postpartum women with abdominal infectious diseases
  • Cardiovascular diseases
  • Previous spinal surgery
  • History of skeletal deformity
  • Participation in any other exercise training program during this study
  • Malignant condition
  • History of acute infection
  • Neurological problems
  • Mental problems preventing evaluation and cooperation
  • Uncontrolled metabolic diseases like diabetes and thyroid disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

the Gynecology and Obstetrics Outpatient clinics, Alexandria University Hospitals, Alexandria, Egypt

Alexandria, Egypt

Actively Recruiting

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Research Team

M

Moaz Khaled Elsayed Mohamed, physical therapist

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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