Status:

ACTIVE_NOT_RECRUITING

Efficacy of Combined Interferential Therapy and Electronic Cupping Therapy for Chronic Constipation Management

Lead Sponsor:

Middle East University

Conditions:

Constipation

Eligibility:

All Genders

20-40 years

Phase:

NA

Brief Summary

Constipation is a common gastrointestinal issue affecting individuals worldwide. Interferential therapy, a form of electrotherapy, has been suggested to have potential benefits in improving gastrointe...

Detailed Description

Objective: The purpose of this study was to assess the effectiveness of a combined treatment regimen that includes interferential therapy and electronic cupping therapy on the symptoms of chronic cons...

Eligibility Criteria

Inclusion

  • history of Chronic Constipation (CC), as defined by either experiencing two or fewer Complete Spontaneous Bowel Movements (CSBMs) per week for a minimum of 6 consecutive months before the screening visit
  • Reporting a sensation of incomplete evacuation or straining during at least a quarter of their bowel movements (according to the generally accepted definition of constipation).
  • Patients must have had CC persisting for more than 6 months, failed to respond to or be intolerant of medical treatment for at least 3 months

Exclusion

  • pregnant or lactating women
  • Chronic Constipation (CC) resulting from anorectal malformations such as colorectal or anal organic lesions, pelvic floor disorders requiring surgical intervention as determined by the investigator (such as rectal prolapse, rectocele, or enterocele)
  • presence of implanted electronic devices like cardiac pacemakers, defibrillators, cardiac pumps, or spinal stimulators
  • CC attributable to medications or neurologic, endocrine, or metabolic conditions
  • prior history of partial colectomy; conditions like megacolon, megarectum, or colonic inertia
  • skin abnormalities that hinder the placement of electrodes
  • women lacking adequate contraception (hormonal or intrauterine device).

Key Trial Info

Start Date :

February 14 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 30 2024

Estimated Enrollment :

110 Patients enrolled

Trial Details

Trial ID

NCT06611852

Start Date

February 14 2023

End Date

November 30 2024

Last Update

September 25 2024

Active Locations (1)

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October 6 university

October City, Giza Governorate, Egypt, 6892