Safety and Efficacy of L-NAME and Midodrine to Increase MAP

NCT ID: NCT00835224

Last Updated: 2014-04-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-05-31
• Study Completion Date: 2013-08-31

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.

Conditions

Orthostatic Hypotension; Spinal Cord Injury

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Midodrine

A drug to treat low blood pressure.

Group Type: EXPERIMENTAL

Midodrine

Intervention Type: DRUG

To treat low blood pressure.

L-Name

L-Name: A non-selective inhibitor of nitric oxide synthase and placebo. It has been used experimentally to induce hypertension.

Group Type: EXPERIMENTAL

L-NAME

Intervention Type: DRUG

A non-selective inhibitor of nitric oxide synthase and placebo. It has been used experimentally to induce hypertension.

Placebo

Placebo: A pill with an inactive substance that looks like the study drug.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

A pill with an inactive substance that looks like the study drug.

Interventions

L-NAME

A non-selective inhibitor of nitric oxide synthase and placebo. It has been used experimentally to induce hypertension.

Intervention Type: DRUG

Midodrine

To treat low blood pressure.

Intervention Type: DRUG

Placebo

A pill with an inactive substance that looks like the study drug.

Intervention Type: DRUG

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

US Department of Veterans Affairs

FED

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jill Wecht, EdD

Role: PRINCIPAL_INVESTIGATOR

VA Medical Center, Bronx

Locations

VA Medical Center, Bronx

The Bronx, New York, United States

Countries

United States

References

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.

Reference Type: RESULT

PMID: 21762873 (View on PubMed)

Other Identifiers

VA Project #5481-08-017

Identifier Type: OTHER

Identifier Source: secondary_id

A6161-W

Identifier Type: -

Identifier Source: org_study_id