NCT04341272View on ClinicalTrials.gov

Intermittent Pneumatic Compression of the Upper Extremity for Post-Operative VTE Prophylaxis

NACompletedINTERVENTIONAL
Enrollment

106

Participants

Timeline

Start Date

April 1, 2014

Primary Completion Date

April 5, 2017

Study Completion Date

April 5, 2017

Conditions
Venous Thromboses
Interventions
DEVICE

Intermittent Pneumatic Compression Device (FDA approved)

Compression Device placed on either upper or lower extremity for DVT prophylaxis following surgery

All Listed Sponsors
lead

Baltimore VA Medical Center

FED

NCT04341272 - Intermittent Pneumatic Compression of the Upper Extremity for Post-Operative VTE Prophylaxis | Biotech Hunter | Biotech Hunter