NCT00732823

Compression Device Safety Study

A Phase II Randomized Study to Evaluate the Safety of the Compression Test Device Using Intermittent Pneumatic Compression Mode in Subjects With Venous Insufficiency and Oedema

• Status: Completed
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 16 (actual)
• Sponsor: ConvaTec Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

To evaluate the safety of the Compression Device to subjects with venous insufficiency and oedema.

Conditions

• Venous Insufficiency

Interventions

Type	Name	Description
DEVICE	Placebo - No device worn
DEVICE	Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs
DEVICE	Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs
DEVICE	Prototype device(unnamed)-A battery operated inflatable pneumatic cuffs

Timeline

• Start date: 2005-07-01
• Primary completion: 2005-10-01
• Completion: 2005-10-01
• First posted: 2008-08-12
• Last updated: 2008-10-31

Locations

1 site across 1 country: Germany