Pneumatic Compression for Preventing Venous Thromboembolism

NACompletedINTERVENTIONAL
Enrollment

2,000

Participants

Timeline

Start Date

July 16, 2014

Primary Completion Date

November 13, 2018

Study Completion Date

November 13, 2018

Conditions
Deep Venous Thrombosis
Interventions
DEVICE

pneumatic compression

All IPC devices intended for DVT prophylaxis are acceptable in the study. Sequential devices (cuffs have several chambers) are preferred, but non-sequential (cuffs have single chambers) are acceptable.

Trial Locations (1)

11426

Intensive Care Unit, King Abdulaziz Medical City, National Guard Health Affairs, Riyadh

All Listed Sponsors
collaborator

King Abdulaziz Medical City, Jeddah

UNKNOWN

collaborator

King Abdulaziz Hospital, Al Ahsa

UNKNOWN

collaborator

Unity Health Toronto

OTHER

collaborator

King Fahad Medical City

OTHER_GOV

collaborator

Assir Central Hospital

UNKNOWN

collaborator

Royal North Shore Hospital

OTHER

collaborator

Mount Sinai Hospital, Canada

OTHER

collaborator

Prince Sultan Military Medical City

OTHER

collaborator

King Faisal Specialist Hospital & Research Center

OTHER

collaborator

Gosford Hospital, Australia

UNKNOWN

collaborator

St Vincent's Hospital - Sydney, Australia

OTHER

collaborator

Medanta, The Medicity, India

OTHER

collaborator

King Fahad Hospital of the University, Al Khobar

UNKNOWN

collaborator

King George's Medical University, India

UNKNOWN

lead

King Abdullah International Medical Research Center

OTHER

NCT02040103 - Pneumatic Compression for Preventing Venous Thromboembolism | Biotech Hunter | Biotech Hunter