NCT00855673

Intermittent Mechanical Compression For Peripheral Arterial Disease

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 30 (actual)
• Sponsor: Hospital Universitario Getafe · Academic / Other
• Sex: All
• Age: 50 Years – 75 Years
• Healthy volunteers: Not accepted

Summary

The study tests the use of a portable mechanical compression device (FM220, Flowmedic, USA) for the treatment of claudication and peripheral arterial disease. Major endpoints are improved exercise tolerance and relevant blood pressure ratios

Conditions

• Peripheral Arterial Disease

Interventions

Type	Name	Description
DEVICE	Intermittent Mechanical Compression	FM220 device
DRUG	Control	Standard medical treatment

Timeline

• Start date: 2001-01-01
• Primary completion: 2007-12-01
• Completion: 2007-12-01
• First posted: 2009-03-04
• Last updated: 2009-03-04