ISRCTN37913976
Completed
未知
A feasibility study to inform the design of a randomised controlled trial to identify the most clinically and cost effective length of anticoagulation with low molecular weight heparin In the treatment of Cancer Associated Thrombosis
Cardiff University (UK)0 sites200 target enrollmentOctober 31, 2012
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Cardiff University (UK)
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
2014 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/24726032 2015 results in: http://www.ncbi.nlm.nih.gov/pubmed/26490434
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Receiving low\-molecular\-weight heparin (LMWH) for treatment of Cancer Associated Thrombosis (CAT) for five months
- •2\. Locally advanced or metastatic cancer
- •3\. Able to self\-administer LMWH, or have LMWH administered by a carer
- •4\. Able to give informed consent
- •5\. Age \=18 years
Exclusion Criteria
- •1\. Receiving drug other than LMWH for CAT
- •2\. Contraindication to anticoagulation
- •2\.1\. Known allergies to LMWHs, heparin, sulfites or benzyl alcohol
- •2\.2\. Active major bleeding
- •2\.3\. History of heparin\-induced thrombocytopenia
- •3\. Confirmed recurrent VTE whilst receiving anticoagulation
- •4\. Female patients who are pregnant
Outcomes
Primary Outcomes
Not specified
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