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To evaluate the effect of capacitive and resistive radiofrequency on postpartum rectus abdominis diastasis.
Eighty females postpartum with rectus diastasis will be included in this study; they will be recruited the outpatient clinic at El Mahalla Al Kobra (The first author's pervious workplace) and will be referred by obstetric and genecology physicians. Patients will be assigned into two groups. Group A: It will include 40 patients participating in abdominal belt. Group B: It will include 40 patients participating in abdominal belt plus TECAR therapy.
Age
20 - 35 years
Sex
FEMALE
Healthy Volunteers
No
Start Date
April 6, 2025
Primary Completion Date
July 7, 2025
Completion Date
August 1, 2025
Last Updated
April 3, 2025
80
ESTIMATED participants
abdominal belt
DEVICE
TECAR therapy
DEVICE
Lead Sponsor
Cairo University
NCT07389993
NCT07233616
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07002944