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Clinical Trial Summary

This project aims to evaluate the physiological effects of Midodrine administration during orthostatic challenge in those with high level spinal cord injury. Midodrine has been shown to improve orthostatic symptoms in those with spinal cord injury but the physiological mechanisms influenced have not been identified. The investigators will examine key physiological components influencing orthostatic tolerance. The investigators will do this, by measuring the baroreflex, and brain blood flow autoregulation (the ability to maintain brain blood flow) before during and after the sit-up test. Two sit-up tests will occur; one before Midodrine administration, and one after administration of a 10mg dose of Midodrine.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01498809
Study type Observational
Source University of British Columbia
Contact
Status Completed
Phase
Start date March 2012
Completion date November 2013

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