Bowel Care and Cardiovascular Function After Spinal Cord Injury
Spinal Cord Injury
About this trial
This is an interventional treatment trial for Spinal Cord Injury focused on measuring spinal cord injury, autonomic dysreflexia, blood pressure, bowel care management, defecation
Eligibility Criteria
Inclusion Criteria:
- traumatic spinal cord injury at least one year ago
- regular bowel care routine (at least four weeks)
Exclusion Criteria:
- cauda equina or conus lesion
- currently use ventilator
- colostomy, or do not perform regular bowel care for any reason
- any skin breakdown (pressure sores)
- do not speak English
- are under 19 years old
- are pregnant or think you might be pregnant
- medical/psychiatric condition or substance abuse that is likely to affect your ability to complete this study
- currently using medications containing lidocaine
- allergy to lidocaine
Sites / Locations
- Simon Fraser University
- International Collaboration on Repair Discoveries
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Lidocaine lubricant (then placebo)
Placebo lubricant (then lidocaine)
In this arm, on the first test day subjects will use lidocaine lubricant in their normal bowel care routine (rather than standard lubricating jelly). After a washout period they will repeat testing with the placebo lubricant.
In this arm, on the first test day subjects will use regular lubricant (AMG MedPro lubricating gel) in their normal bowel care routine. After a washout period they will repeat testing with a the lidocaine lubricant.