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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02398266
Other study ID # Sonazoid in PAD
Secondary ID
Status Recruiting
Phase Phase 2
First received March 3, 2015
Last updated June 16, 2017
Start date August 1, 2016
Est. completion date July 1, 2018

Study information

Verified date June 2017
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The measurement of limb skeletal muscle perfusion and perfusion reserve during exercise is an approach that can assess the total impact of the complex pathophysiologic processes in patients with limb ischemia, particularly in those with diabetes in whom distal arterial disease and abnormal microvascular functional responses are common. This trial is designed to: (a) optimize methods for assessment of limb perfusion at rest and during stress using contrast-enhanced ultrasound (normal subjects) and a microbubble contrast agent that is able to provide non-linear signal without destruction at medium acoustic pressures, and (b) to test whether perfusion imaging provides incremental information on the severity of disease in patients with peripheral artery disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 55
Est. completion date July 1, 2018
Est. primary completion date July 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

- For Healthy controls: no active major medical problems or vasoactive medications

- For PAD: Known diagnosis with PAD an ABI of 0.4-0.6

Exclusion Criteria:

- Rutherford class 6 or greater

- Allergy to ultrasound contrast agents

- Previous limb amputation

- Pregnancy

- Known congenital or acquired right to left shunt

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Contrast ultrasound of leg muscle with Sonazoid (Contrast ultrasound microvascular perfusion imaging)
Skeletal muscle perfusion assessment of the thigh and calf skeletal muscle will be performed with contrast ultrasound of leg muscle with Sonazoid while at rest and during exercise stress

Locations

Country Name City State
United States Oregon Health & Science University Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skeletal muscle perfusion as measured by contrast ultrasound with Sonazoid microbubbles 5 minutes
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