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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01573169
Other study ID # PREVENTIHS
Secondary ID
Status Terminated
Phase Phase 3
First received
Last updated
Start date May 2012
Est. completion date March 2020

Study information

Verified date September 2021
Source University Of Perugia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with cerebral hemorrhage (ICH) have a high risk of venous thromboembolism. Intermittent pneumatic compression combined with elastic stockings have been shown to be superior to elastic stockings alone in reducing the rate of asymptomatic deep vein thrombosis after ICH in a randomized trial (4.7% vs. 15.9%). Graduated compression stockings alone are ineffective in preventing deep vein thrombosis in patients with ischemic or hemorrhagic stroke. Less clear is the role of anticoagulation in the prevention of venous thromboembolism in patients with ICH because the use of anticoagulants may cause an enlargement of the hematoma. In a multicenter, randomized trial, the investigators will assess the efficacy and safety of enoxaparin in the prevention of venous thromboembolism in patients with spontaneous intracerebral hemorrhage. Enoxaparin (40 mg once daily) or standard therapy (graduated compression stockings and/or intermittent pneumatic compression and/or early mobilization) will be given subcutaneously for not less than 10 days beginning after 72 hours from stroke onset.


Recruitment information / eligibility

Status Terminated
Enrollment 73
Est. completion date March 2020
Est. primary completion date March 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Intracranial spontaneous hemorrhage on brain CT scan - Intracranial hemorrhage during treatment with oral anticoagulants - Bedridden patients (item 6 of NIHSS: motor leg points 3 or 4 or severe ataxia for cerebellar hemorrhage). Exclusion Criteria: - cerebral hemorrhage due to intracranial vascular malformation - rebleeding on CT scan after 72 hours from stroke (before randomization)

Study Design


Intervention

Drug:
Enoxaparin
enoxaparin 0.4 ml sc per day for 10 days started 72 hours after the stroke
Other:
Graduated compression stockings and/or intermittent pneumatic compression and/or early mobilization
placebo standard therapy

Locations

Country Name City State
Italy Stroke Unit Perugia

Sponsors (1)

Lead Sponsor Collaborator
University Of Perugia

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Paciaroni M, Agnelli G, Venti M, Alberti A, Acciarresi M, Caso V. Efficacy and safety of anticoagulants in the prevention of venous thromboembolism in patients with acute cerebral hemorrhage: a meta-analysis of controlled studies. J Thromb Haemost. 2011 May;9(5):893-8. doi: 10.1111/j.1538-7836.2011.04241.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With Symptomatic and Asymptomatic Venous Thromboembolism Symptomatic venous thromboembolism (deep venous thrombosis and/or pulmonary embolism) and asymptomatic deep venous thrombosis on ultrasound examination 10 days
Secondary Bleedings symptomatic and asymptomatic intra and extracranial bleedings 90 days
Secondary Mortality mortality of any cause 90 days
Secondary Disability modified Rankin Scale (mRS) equal to and greater than 3.
0 - No symptoms.
- No significant disability. Able to carry out all usual activities, despite some symptoms.
- Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities.
- Moderate disability. Requires some help, but able to walk unassisted.
- Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted.
- Severe disability. Requires constant nursing care and attention, bedridden, incontinent.
- Dead.
90 days
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