Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02478671
Other study ID # TIS2015-002
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 19, 2015
Last updated June 24, 2015
Start date June 2015
Est. completion date August 2015

Study information

Verified date June 2015
Source Terumo Medical Corporation
Contact Jodie A Ruffing, ADN, BSBA
Email jodie.ruffing@terumomedical.com
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Subjects' radial artery diameters and plethsmography waveforms will be recorded by MRI and pulse oxymetry at varying levels of radial artery compression by the Terumo TR Band.


Description:

In this study, the diameter of each subjects' radial artery will be measured using MRI imagery at varying degrees of radial artery compression by adjusting the amount of air injected into a Terumo TR Band. In addition, using pulse oxymetery, the perfusion waveform will be measured and recorded also while the subjects have a TR Band in place on their wrists.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 4
Est. completion date August 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Female or male adult (has reached the legal majority age).

2. Subject has provided his/her written informed consent to participate in the trial prior to any study -related procedure being conducted.

Exclusion Criteria:

1. Abnormal result of either baseline Barbeau or reverse Barbeau tests.

2. Pregnant or breast feeding female.

3. Subject with contraindication to MRI

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Device:
TR Band
The radial artery will be compressed using a Terumo TR Band and artery diameter and perfusion will be measured

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Terumo Medical Corporation Medical University of South Carolina

Outcome

Type Measure Description Time frame Safety issue
Primary Radial artery compression measured using MRI measure degree of artery compression while TR Band is in place Subjects will be followed up to one week post procedure No
Secondary Hand perfusion as measured by pulse oxymetry waveform pulse oxymetry waveform will be used to measure arterial perfusion Subjects will be followed up to one week post procedure No
See also
  Status Clinical Trial Phase
Not yet recruiting NCT01532505 - Effect of Vasopressin on Tissue Oxygen Saturation in Cardiac Surgery Patients During Cardiopulmonary Bypass N/A
Completed NCT01852461 - Perfusion Index Variability in Respiratory Distress Syndrome N/A