NCT00732823View on ClinicalTrials.gov

Compression Device Safety Study

PHASE2CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

July 31, 2005

Primary Completion Date

October 31, 2005

Study Completion Date

October 31, 2005

Conditions
Venous Insufficiency
Interventions
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

Trial Locations (1)

Unknown

Hautarzt Phlebologe Allergologe, Freiburg im Breisgau

Sponsors

Lead Sponsor

ConvaTec Inc.

Collaborators (1)

Bristol-Myers Squibb
All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

lead

ConvaTec Inc.

INDUSTRY