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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04510974
Other study ID # WEC-18-025
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date June 30, 2018
Est. completion date December 1, 2020

Study information

Verified date August 2020
Source James J. Peters Veterans Affairs Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study is examining differences in central arterial stiffness, orthostatic changes in blood pressure, norepinephrine, and plasma renin in individuals with spinal cord injury compared with age-matched uninjured controls.


Description:

The study is examining differences in central arterial stiffness, orthostatic changes in blood pressure, norepinephrine, and plasma renin in individuals with spinal cord injury compared with age-matched uninjured controls. Arterial stiffness and blood pressure will be collected in the laying down position. A blood sample of norepinephrine and plasma renin will also be collected. The participant will tilt to 30, 45 and 60 degrees for 10 minutes at each angel. Blood pressure and heart rate will be monitored at each angle. Another blood sample of renin and norepinephrine will be collected at the end of 10 minutes at 60 degrees.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 33
Est. completion date December 1, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers
Gender All
Age group 21 Years to 70 Years
Eligibility Inclusion Criteria:

- SCI participants:

- injured between C1-T1 and T6-T12

- wheelchair dependent

- AIS classification A, B or C

- Injured occurred more than 1 year ago

Exclusion Criteria:

- currently have an illness or infection

- current smoker of at least 1 year

- controlled or uncontrolled hypertension or diabetes mellitus

- Neurological condition other than SCI (Alzheimer's disease, dementia, stroke, multiple sclerosis, Parkinson's disease)

- cardiovascular disease (coronary heart disease, congestive heart failure, peripheral artery disease)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Spinal Cord Injury
Spinal Cord Injury

Locations

Country Name City State
United States James J Peters VAMC Bronx New York

Sponsors (3)

Lead Sponsor Collaborator
James J. Peters Veterans Affairs Medical Center Kessler Foundation, Seton Hall University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pulse wave velocity (m/s) Determine relationship between arterial stiffness, blood pressure, norepinephrine, and renin responses to head-up tilt among the groups. 2 years
Secondary Systolic Blood Pressure (mmHg) Determine differences in blood pressure among groups 2 years
Secondary Plasma renin (pg/ml) Determine differences in plasma renin among the groups 2 years
Secondary Norepinephrine (pg/ml) Determine differences in plasma norepinephrine among the groups. 2 years
Secondary Norepinephrine and Renin Describe the changes in norepinephrine and renin from supine rest to 60 degree tilt 2 years
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