N/A
N=152
Using Intravenous Heparin Versus Standard of Care Subcutaneous Heparin to Prevent Clots After Surgery
Venous Thrombosis
Bottom Line
View on ClinicalTrials.gov: NCT01608906 ↗Enrolled (actual)
152
Serious AEs
0.0%
Results posted
Jul 2021
Primary outcome: Primary: Development of DVT (Deep Vein Thrombosis)
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- low dose intravenous heparin (LDIVH) (Drug); Heparin (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Colorado, Denver
- Primary completion
- May 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Development of DVT (Deep Vein Thrombosis) |
— | — |
| SECONDARY Development of PE's; Sepsis |
— | — |
Summary
This study plans to learn more about what is the best treatment to prevent blood clots in patients in intensive care units (ICU's). The investigators know that patients who are in ICU's have a higher than normal risk of getting blood clots in the veins of their arms or legs. This can be very dangerous as the clot may move into the lungs. To prevent this, the standard treatment is to give low dose heparin subcutaneously 3 times a day (usually 5000 units at each dose). In this study the investigators are randomizing patients to receive either standard of care or low dose intravenous heparin in a continuous infusion.
Eligibility Criteria
Inclusion Criteria
- A signed informed consent;
- Age between 18 and 80 years
- The patient is admitted to the surgical intensive care unit at the University of Colorado Hospital
Exclusion Criteria
- Predicated SICU stay less than 5 days;
- Pregnancy;
- Breast feeding;
- Initial platelet count < 30,000;
- Currently eligible for treatment of thromboembolism;
- Prior organ transplant;
- Cardiopulmonary bypass within previous 30 days;
- Advanced directive precluding participation;
- Already receiving pharmacologic agent for DVT prophylaxis;
- Prior diagnosis of heparin-induced thrombocytopenia;
- Heparin allergy
Data sourced from ClinicalTrials.gov (NCT01608906). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.