EXCLAIM:Extended Prophylaxis for Venous ThromboEmbolism (VTE) in Acutely Ill Medical Patients With Prolonged Immobilization

Completed · Phase 4

Conditions studied: Venous Thromboembolism

In brief

Primary objective: * To demonstrate the superiority of extended VTE prophylaxis with enoxaparin 40mg sc qd for 28 ± 4 days, compared to placebo, both following 10 ± 4 days of initial treatment with enoxaparin 40mg sc qd Secondary objectives: * To assess the reduction in mortality rate at the end of the double-blind treatment period, at 3 (90 ± 10 days) and at 6 (180 ± 10 days) months from the time of entry to the study, in patients on extended prophylaxis * To assess the incidence of VTE at 3 months (90 ± 10 days) from the time of randomization to the study * To evaluate the safety of extended enoxaparin VTE prophylaxis in acutely ill medical patients with prolonged immobilization. Safety evaluation includes: * Major and minor hemorrhage * Heparin induced thrombocytopenia * Serious adverse events * To assess differences in levels of health-care utilization and cost between patients receiving extended VTE prophylaxis versus those receiving placebo.

Key facts

Study ID

NCT00077753

Run by

Sanofi

People needed

4726

Starts

2002-02-01

Expected to finish

2007-02-01

Last updated by the study team

2011-01-11

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Recent immobilization ≤ 3 days
• Level 1 mobility patients who are ≥ 40 years of age with acute medical illness or acute exacerbation of chronic medical illness
• Level 2 mobility patients who
• are >75 yrs of age
• are ≥ 40 years of age and have a history of VTE (deep venous thrombosis or pulmonary embolism)
• are ≥ 40 years of age and have a baseline diagnosis of cancer (active cancer or history of cancer)
• Anticipated decreased level of mobility of 5 ± 2 days with a level of activity 1 and 2 at the time of study entry and likely to continue at a lower than pre-morbid activity level after the initial 5 ± 2 day period. PATIENTS DO NOT HAVE TO BE HOSPITALIZED IN ORDER TO BE INCLUDED IN THE STUDY.(Definition of decreased level of mobility: _Level 1:bed rest or sedentary patients _Level 2:level 1 with bathroom privileges)
• Presence of at least one of the following medical conditions:
• Heart Failure, NYHA class III and IV
• Class III : Patients with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitationdyspnea, or anginal pain.
• Class IV : Patients with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.
• Acute respiratory insufficiency
• Other acute medical conditions such as:
• Acute ischemic stroke, any territory, with an appropriate neuroradiologic (head CT scan or brain MRI scan) providing results consistent with non hemorrhagic stroke
• acute infection without septic shock
• acute rheumatic disorders
• active episode of inflammatory bowel disease
• active cancer defined as history of histologically or cytologically confirmed cancer in patients who are not candidates for debulking or curative intent surgery at study entry
• Any other acute medical illness or exacerbation of chronic medical illness resulting in clinically significant reduction in mobility as compared to premorbid level.

You may not qualify if…

• Women who are breastfeeding, pregnant or of childbearing age and not using medically acceptable effective contraception
• Patients with any evidence of an active bleeding disorder
• Contraindication to anticoagulation
• Major surgery within the previous 3 months
• Patients who have had spinal or epidural analgesia or lumbar puncture within the preceding 24 hours
• Known hypersensitivity to heparin, or LMWH, or pork derived products
• A documented previous episode of heparin-induced or LMWH induced thrombocytopenia and/or thrombosis (HIT, HAT, or HITTS)
• Patients who have taken part in another clinical trial within the previous thirty days
• Patients with a persistent renal failure. The patient's creatinine level must be less than the creatinine level per gender/age/weight. This will replace the calculated creatinine clearance
• Known or suspected severe anemia of unexplained cause considered clinically relevant by investigator
• Patients with prosthetic heart valves
• Patients with known cerebral metastases

Where it is running

• Sanofi-Aventis — Bridgewater, New Jersey, United States
• Sanofi-Aventis — Buenos Aires, Argentina
• Sanofi-Aventis — North Ryde, Australia
• Sanofi-Aventis — Vienna, Austria
• Sanofi-Aventis — Brussels, Belgium
• Sanofi-Aventis — São Paulo, Brazil
• Sanofi-Aventis — Laval, Canada
• Sanofi-Aventis — Bogotá, Colombia
• Sanofi-Aventis — Paris, France
• Sanofi-Aventis — Berlin, Germany
• Sanofi-Aventis — Mumbai, India
• Sanofi-Aventis — Netanya, Israel
• Sanofi-Aventis — Milan, Italy
• Sanofi-Aventis — México, Mexico
• Sanofi-Aventis — Warsaw, Poland
• Sanofi-Aventis — Moscow, Russia
• Sanofi-Aventis — Johannesburg, South Africa
• Sanofi-Aventis — Barcelona, Spain
• Sanofi-Aventis — Mégrine, Tunisia
• Sanofi-Aventis — Guildford, United Kingdom

Full record on ClinicalTrials.gov

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