NL-OMON32323
Completed
Not Applicable
Efficacy and safety of home treatment versus in hospital treatment with LMWH in patients with non-massive pulmonary embolism - The Hestia Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pulmonary embolism
- Sponsor
- GlaxoSmithKline
- Enrollment
- 280
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Consecutive patients with proven acute non\-massive, stable PE
- •2\. Age over 18
- •3\. Informed consent
Exclusion Criteria
- •1\. Patients who have had symptoms of PE for longer than 7 days duration
- •2\. Diagnosis of PE during anticoagulant treatment
- •3\. Active bleeding, or a very high risk for major bleeding
- •4\. Severe pain requiring intravenous narcotic analgesia
- •5\. Medical or social condition which necessitates admission to the hospital for another reason
- •6\. Pregnancy
- •7\. Severe renal of liver failure
- •8\. Previously documented heparin induced thrombocytopenia
Outcomes
Primary Outcomes
Not specified
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