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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03423316
Other study ID # 2019P001781
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 31, 2020
Est. completion date July 2021

Study information

Verified date September 2020
Source Massachusetts General Hospital
Contact Lei Zhang
Phone 6177268627
Email jeff.zhang@mgh.harvard.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this project, the investigators propose to use high-resolution magnetic resonance imaging (MRI) to measure blood perfusion in different groups of calf muscle. This imaging approach is standard of care for evaluation of coronary artery disease (CAD), and has never been successfully applied to PAD. Preliminary results show distinct patterns of muscle perfusion between healthy and PAD patients, and thus great promise of the technique. The investigators will first verify the reproducibility of the technique, and then compare the calf muscle perfusion measures in PAD patients against healthy age-matched controls. This comparison will test the feasibility of detecting functional abnormality in PAD patients. After the baseline scans, the PAD patients will opt to undergo a 12-week supervised exercise therapy, and then a post-therapy MRI scan. Comparison of the pre- and post-therapy measurements will indicate how the therapy improves the calf-muscle perfusion, and how this perfusion change correlates with increases in patient's walking ability.

The long term goals of this project are to develop an improved diagnostic test for patients with PAD to predict who will benefit from therapeutic intervention. The MRI perfusion studies of calf muscle can be performed in conjunction with routine peripheral MR angiography to assess the functional significance of vascular stenosis.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 90
Est. completion date July 2021
Est. primary completion date July 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

PAD patients with

- Intermittent claudication

- Ankle-brachial blood-pressure index (ABI) < 0.9

Exclusion Criteria:

- Estimated glomerular filtration rate (eGFR) < 30 ml/min/1.73m2

- Chronic pulmonary diseases

- Arthritis or other joint ailments

Study Design


Intervention

Behavioral:
Supervised exercise therapy
The therapy will be conducted three times each week for 12 weeks. Each session takes 1 hour, consisting of 5 minutes of warmup activities, 50 minutes of intermittent exercise, and 5 minutes of cool-down activities. Exercise consists of walking on a treadmill initiated at 2 mph and 0% grade, until claudication pain becomes moderately severe. After claudication pain subsides, the subject will restart the walk. At the end of the session, the total exercise duration will be recorded. After a patient is able to walk 8-10 minutes at the initial workload, the grade is increased by 1-2%, or the speed is increased by 0.5 mph as tolerated.

Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stress-rest calf-muscle perfusion Perfusion in the different calf muscle groups following exercises of low (rest) and high (stress) intensities Single visit (~90 minutes)
Primary Perfusion changes following supervised exercise therapy Change in stress-rest calf-muscle perfusion in PAD patients following the 12-week supervised exercise therapy Before and after supervised exercise therapy (12 weeks)
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