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| Sponsored by: |
Department of Veterans Affairs |
| Information provided by: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00013312 |
Purpose
This study will compare individuals with acute SCI to control patients in order to: 1. Determine if there are changes in colonic tone and sensation after SCI by comparing the fasting responses to the postprandial responses; 2. Determine if there are changes in colonic phasic motility after SCI by comparing the fasting responses to the postprandial responses; 3. Determine if colonic motor and sensory function after SCI change over time by repeating these studies six month later in SCI and control patients.
| Condition | Intervention | Phase |
|
Spinal Cord Injury |
Procedure: Determine colonic tone |
Phase II |
| MedlinePlus related topics: | Spinal Cord Injuries |
| Study Type: | Interventional |
| Study Design: | Diagnostic, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study |
| Official Title: | Effects of Acute SCI on Colonic Motility & Tone |
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Acute SCI with impaired colonic tone
Contacts and Locations| United States, Illinois | |||||
| VAMC, Hines | |||||
| Hines, Illinois, United States | |||||
| Investigator: | John Fryer, Ph.D. Asst. Director | Department of Veterans Affairs, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service |
| Investigator: | Nancy Rocheleau, Program Analyst | Department of Veterans Affairs, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service |
More Information
| Study ID Numbers: | B1862R |
| First Received: | March 14, 2001 |
| Last Updated: | December 12, 2007 |
| ClinicalTrials.gov Identifier: | NCT00013312 |
| Health Authority: | United States: Federal Government |
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