NCT00732719View on ClinicalTrials.gov

Compression Device Safety Study on Edema

PHASE2CompletedINTERVENTIONAL

Enrollment

12

Participants

Timeline

Start Date

October 31, 2004

Primary Completion Date

November 30, 2004

Study Completion Date

December 31, 2004

Conditions

Edema

Interventions

DEVICE

Prototype device (unnamed) worn-no pressure given (placebo) from inflatable cuffs

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

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

Collaborators (1)

Bristol-Myers Squibb

All Listed Sponsors

lead

ConvaTec Inc.

INDUSTRY

collaborator

Bristol-Myers Squibb

INDUSTRY

NCT00732719 - Compression Device Safety Study on Edema | Biotech Hunter | Biotech Hunter