Prophylaxis In Venous Thromboembolism In Primary Care, A Pilot Study

PHASE4TerminatedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

April 30, 2003

Study Completion Date

December 31, 2003

Conditions
ThromboembolismDeep Vein ThrombosisDalteparin
Interventions
DRUG

Dalteparin sodium

Dalteparin sodium was administered at a daily dosage of 5,000 UI anti-Xa by subcutaneous route. The treatment duration was 7 days in a single daily injection throughout the bedridden period.

DRUG

Placebo

Placebo was administered with a daily injection of 0.2 mL by subcutaneous route. The treatment duration was 7 days in a single daily injection throughout the bedridden period.

Trial Locations (5)

24005

Pfizer Investigational Site, León

28001

Pfizer Investigational Site, Madrid

29620

Pfizer Investigational Site, Torremolinos

Unknown

Pfizer Investigational Site, Madrid

Pfizer Investigational Site, Parla

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY