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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06078176
Other study ID # B4529-R
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2024
Est. completion date December 31, 2026

Study information

Verified date March 2024
Source VA Office of Research and Development
Contact Dennis Bourbeau, PhD
Phone (216) 791-3800
Email Dennis.Bourbeau@va.gov
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators are testing the effect of electrical stimulation of the rectum on colonic motility. Most individuals with spinal cord injury develop neurogenic bowel dysfunction, which includes slowed colonic motility, which means that stools take longer than normal to pass through the colon. This slowed movement may result in chronic constipation and difficulty emptying the bowels. Individuals typically (without or without caregiver assistance) insert a gloved finger into the rectum and gently stretch it to improve colonic motility for a brief period to empty the bowels. The investigators hypothesize that electrically stimulating the rectum, instead of mechanically stretching it, will produce the same beneficial effect of improving colonic motility. Therefore, this study will compare the two methods. If electrical stimulation effectively improves colonic motility, then the investigator shall develop the approach as a therapeutic intervention in future studies.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 12
Est. completion date December 31, 2026
Est. primary completion date December 31, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Suprasacral spinal cord injury - Diagnosed neurogenic bowel dysfunction and using digital rectal stimulation - Bowel routine requires at least 30 minutes or at least 3 cycles of digital rectal stimulation - Neurologically stable - At least 18 years old - At least 12 months post neurological injury or disease diagnosis Exclusion Criteria: - Active sepsis - Open pressure sores on or around pelvis - Significant colon trauma or colostomy - Crohn's disease - Colonic obstruction or gastrointestinal surgery within last 3 months - Significant history of autonomic dysreflexia

Study Design


Intervention

Other:
Electrical Rectal Stimulation
Electrical stimulation of the rectum will be applied to activate sensory afferent neurons of the rectum and evoke a recto-colonic reflex to improve colonic motility and facilitate bowel emptying. This intervention will compared to individuals' usual mechanical intervention of digital rectal stimulation.

Locations

Country Name City State
United States Louis Stokes VA Medical Center, Cleveland, OH Cleveland Ohio
United States Syracuse VA Medical Center, Syracuse, NY Syracuse New York

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time required to complete bowel emptying Two interventions will be tested, including the clinical standard of digital rectal stimulation and a novel approach using electrical stimulation of rectal sensory afferents, to determine the effect on colonic pressure. We will compare the time required for the participant to complete their bowel emptying routine between a control period with digital rectal stimulation and a treatment period with electrical rectal stimulation. 12 weeks
See also
  Status Clinical Trial Phase
Recruiting NCT04127617 - Effects of Osteopathic Manipulative Treatment in People With Neurogenic Bowel Dysfunction N/A
Completed NCT02641483 - Stimulation for Colonic Motility N/A