Safety and Efficacy of L-NAME and Midodrine to Increase MAP
Primary Purpose
Orthostatic Hypotension, Spinal Cord Injury
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
L-NAME
Midodrine
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Orthostatic Hypotension focused on measuring Spinal Cord Injury, Orthostatic Hypotension, Blood Pressure, Midodrine Hydrochloride, L-NAME
Eligibility Criteria
Inclusion Criteria:
Spinal Cord Injured Subjects:
- chronic spinal cord injury (1 year post injury) with a seated MAP of 65mmHg (almost all individuals with tetraplegia demonstrate this)
- Male or female with an age of 18 - 65 years
Control Subjects:
- Male or female with an age of 18 - 65 years
Exclusion Criteria:
Spinal Cord Injured Subjects:
- acute illness
- cardiovascular disease
- renal disease
- medications that affect the cardiovascular system
Control Subjects:
- acute illness
- cardiovascular disease
- renal disease
- medications that affect the cardiovascular system
Sites / Locations
- VA Medical Center, Bronx
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Midodrine
L-Name
Placebo
Arm Description
A drug to treat low blood pressure.
L-Name: A non-selective inhibitor of nitric oxide synthase and placebo. It has been used experimentally to induce hypertension.
Placebo: A pill with an inactive substance that looks like the study drug.
Outcomes
Primary Outcome Measures
Blood Pressure
Secondary Outcome Measures
Full Information
NCT ID
NCT00835224
First Posted
January 30, 2009
Last Updated
March 21, 2014
Sponsor
US Department of Veterans Affairs
1. Study Identification
Unique Protocol Identification Number
NCT00835224
Brief Title
Safety and Efficacy of L-NAME and Midodrine to Increase MAP
Official Title
Safety and Efficacy of L-NAME and Midodrine to Increase MAP in Persons With Tetraplegia
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
August 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
After a spinal cord injury the brain is no longer completely in control of the body below the level of injury. This affects many organs and systems in the body, we are interested in understanding how a spinal cord injury affects blood pressure and blood flow to the brain. We are going to study blood pressure while the person is seated in a wheelchair before and after we give the subject medications which should increase blood pressure in a laboratory setting and over the course of a normal day in persons with spinal cord injury.
Detailed Description
Blood pressure regulation is compromised in persons with tetraplegia due to de-centralization of sympathetic cardiovascular control, associated with hypotension during upright positioning (7, 10, 18, 33). An alpha receptor agonist (midodrine hydrochloride) has been reported to raise blood pressure in persons with tetraplegia (25, 26, 30). Midodrine is the only drug that is presently available to treat orthostatic hypotension. In the clinical armamentarium, it is always beneficial to have agents from multiple drug classes to treat a condition. In the treatment of hypertension, several classes of drugs may be prescribed to lower blood pressure, alone or in combination. The clinician and patient would benefit if another class of drug, with a totally separate mechanism of action, were available to treat orthostatic hypotension. A nitric oxide synthase inhibitor (NOSi), nitro-L-arginine methyl ester (L-NAME), has been shown by our group to "normalize" blood pressure in persons with tetraplegia (32). The safety and efficacy of these two hypertensive agents has not been investigated or compared in persons with chronic tetraplegia. Although the mechanism of action of each of these agents is appreciated, the relative cardiovascular effect in persons with SCI compared with controls is not known. The study will determine the efficacy and safety of these two medications at restoring mean arterial pressure (MAP) during daily activities in persons with chronic tetraplegia. Furthermore, the implication of restoring MAP to normal levels (80 10 mmHg) in individuals with tetraplegia on cardiovascular, autonomic, hormonal and cognitive function.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Orthostatic Hypotension, Spinal Cord Injury
Keywords
Spinal Cord Injury, Orthostatic Hypotension, Blood Pressure, Midodrine Hydrochloride, L-NAME
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Midodrine
Arm Type
Experimental
Arm Description
A drug to treat low blood pressure.
Arm Title
L-Name
Arm Type
Experimental
Arm Description
L-Name: A non-selective inhibitor of nitric oxide synthase and placebo. It has been used experimentally to induce hypertension.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo: A pill with an inactive substance that looks like the study drug.
Intervention Type
Drug
Intervention Name(s)
L-NAME
Intervention Description
A non-selective inhibitor of nitric oxide synthase and placebo. It has been used experimentally to induce hypertension.
Intervention Type
Drug
Intervention Name(s)
Midodrine
Intervention Description
To treat low blood pressure.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
A pill with an inactive substance that looks like the study drug.
Primary Outcome Measure Information:
Title
Blood Pressure
Time Frame
Blood pressure during the 4 hour period after no drug, L-NAME (IV: 1.0 mg/kg) and midodrine (PO: 10.0 mg) administration
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Spinal Cord Injured Subjects:
chronic spinal cord injury (1 year post injury) with a seated MAP of 65mmHg (almost all individuals with tetraplegia demonstrate this)
Male or female with an age of 18 - 65 years
Control Subjects:
Male or female with an age of 18 - 65 years
Exclusion Criteria:
Spinal Cord Injured Subjects:
acute illness
cardiovascular disease
renal disease
medications that affect the cardiovascular system
Control Subjects:
acute illness
cardiovascular disease
renal disease
medications that affect the cardiovascular system
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jill Wecht, EdD
Organizational Affiliation
VA Medical Center, Bronx
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Medical Center, Bronx
City
Bronx
State/Province
New York
ZIP/Postal Code
10468
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
21762873
Citation
Wecht JM, Radulovic M, Rosado-Rivera D, Zhang RL, LaFountaine MF, Bauman WA. Orthostatic effects of midodrine versus L-NAME on cerebral blood flow and the renin-angiotensin-aldosterone system in tetraplegia. Arch Phys Med Rehabil. 2011 Nov;92(11):1789-95. doi: 10.1016/j.apmr.2011.03.022. Epub 2011 Jul 16.
Results Reference
result
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Safety and Efficacy of L-NAME and Midodrine to Increase MAP
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