Time comparison of bowel programs in spinal cord injury

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will compare three bowel-management options—suppository, Enemeez mini enema, and Peristeen transanal irrigation—to see which one lets patients finish their bowel program fastest. The study uses three sequential cohorts, each month assigning a different intervention to participants starting their bowel program. Outcomes include time spent on the bowel program, episodes of incontinence or constipation, and user satisfaction. The trial aims to inform clinical practice to reduce caregiver burden and improve patient experience in neurogenic bowel management after spinal cord injury. Conducted at Casa Colina Hospital, the study will enroll adults with reflexic neurogenic bowel admitted to the inpatient rehab unit.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* admission to acute rehab inpatient unit
* diagnosis of spinal cord injury
* reflexive type neurogenic bowel requiring bowel program with suppository and digital stimulation

Exclusion Criteria:

* anal or rectal stenosis
* active inflammatory bowel disease
* acute diverticulitis
* colorectal cancer
* ischemic colitis
* rectal surgery within the last 3 months
* endoscopic polypectomy within the last 4 weeks
* areflexic bowel
* severe autonomic dysreflexia

Where it's running

• Casa Colina Hospital and Centers for Healthcare
  Pomona, California, United States Recruiting

Study contacts

• Study coordinator: Megan Narintarangkool
• Email: mnarintarangkool@casacolina.org
• Phone: (909)596-7733

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Implanted Brain-Computer Interface to Help People with Severe Arm Impairment

  We’re testing the N1 System, a fully implanted brain interface in the motor cortex with a robot, to see if it can help adults with spinal cord injury, ALS, or chronic stroke use a computer or keyboard more easily.

  Recruiting Neuralink Corp · Miami, Florida · NCT07929792

• tSCS with rehabilitation for improving movement after spinal cord injury

  This study tests whether adding rehabilitation training to transcutaneous spinal cord stimulation helps paraplegic patients regain voluntary movement after spinal cord injury.

  Recruiting Beijing Tsinghua Chang Gung Hospital · Beijing · NCT07907952

• Informational Needs of Caregivers of Patients in Neuro Rehab: Validating the QBI-R/V

  This study tests a caregiver questionnaire (QBI-R and QBI-V) to see how well it measures caregivers’ informational needs during neuromotor rehabilitation.

  Recruiting at 13 sites Istituti Clinici Scientifici Maugeri SpA · Sciacca, Agrigento and 12 other locations · NCT07903298

• Biomechanical and Perceived Effort in Manual Wheelchair Propulsion

  This study tests whether combining objective shoulder loading data with how hard people feel they’re working can reveal how difficult manual wheelchair propulsion is for users with spinal cord injury.

  Recruiting Centre Médico-Chirurgical de Réadaptation des Massues Croix Rouge Française · Lyon · NCT07897214

• Shockwave therapy added to toxin injections to help spasticity after spinal cord injury

  Aims to see if focused shockwave therapy plus Botox injections reduce spasticity better than Botox alone in adults with spinal cord injury.

  Recruiting Phase 2 Kessler Foundation · West Orange, New Jersey · NCT07894991

• Vibratory Genital Nerve Stimulation to Help Female Sexual Function After Spinal Cord Injury

  This study tests whether a home-use vibration device can improve sexual function in cisgender women with spinal cord injury by increasing genital blood flow during arousal.

  Recruiting Hennepin Healthcare Research Institute · Minneapolis, Minnesota · NCT07870642

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.