NCT04250675View on ClinicalTrials.gov

Intermittent Pneumatic Compression to Improve Revascularization Outcome

NACompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

February 1, 2020

Primary Completion Date

December 31, 2022

Study Completion Date

December 31, 2022

Conditions
Peripheral Arterial Disease
Interventions
DEVICE

Intermittent pneumatic leg compressions

Patients will be asked to use the ArtAssist® device to compress the foot and ankle (120 mmHg) of both legs for 2 hours daily for 3 months.

DEVICE

Sham

Patients will be asked to use the ArtAssist® device to compress the foot and ankle (30 mmHg) of both legs for 2 hours daily for 3 months.

Trial Locations (1)

46202

IU Health Methodist, Indianapolis

All Listed Sponsors
collaborator

Roseguini, Bruno, PhD

INDIV

lead

Indiana University

OTHER

NCT04250675 - Intermittent Pneumatic Compression to Improve Revascularization Outcome | Biotech Hunter | Biotech Hunter