Clinical Trials Directory

Trials / Completed

CompletedNCT01498809

Blood Pressure and Brain Blood Flow Regulation After Midodrine Administration in Those With Spinal Cord Injury

Neural and Mechanical Baroreflex Sensitivity and Cerebral Blood Flow

Status
Completed
Phase
Study type
Observational
Enrollment
22 (actual)
Sponsor
University of British Columbia · Academic / Other
Sex
All
Age
18 Years – 49 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGMidodrineSingle 10 mg dose

Timeline

Start date
2012-03-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2011-12-23
Last updated
2019-10-01

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01498809. Inclusion in this directory is not an endorsement.

Blood Pressure and Brain Blood Flow Regulation After Midodrine Administration in Those With Spinal Cord Injury (NCT01498809) · Clinical Trials Directory