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Comparison of intravenous enoxaparin with subcutaneous enoxaparin in preventing venous thromboembolism

Comparison of intravenous enoxaparin with subcutaneous enoxaparin in preventing venous thromboembolism in patients admitted to intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191012045075N1
Enrollment
20
Registered
2020-01-26
Start date
2013-09-23
Completion date
Unknown
Last updated
2020-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intravenous thromboembolism.

Interventions

Intervention 1: In the first group, 0.5 mg/kg of enoxaparin (AVENTIS PHARMA Co., France) was injected subcutaneously in the deltoid region and rotationally the internal surface of the groin on both si

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Ages 18 to 70 years Hospitalization for at least 48 hours in ICU Mechanical ventilation Normal renal and hepatic function Passing 48 hours from surgery in patients with intracerebral hemorrhage (epidural , subdural and intracerebral hematoma and hemorrhagic stroke)

Exclusion criteria

Exclusion criteria: History of deep vein thrombosis History of pulmonary embolism History of coagulation disorders (hemophilia, disseminated intravascular coagulation, idiopathic thrombocytopenia, heparin- induced thrombocytopenia and disruption of coagulation tests) Treated with other anticoagulants before hospitalization Prosthetic implantation (artificial heart valve, stent and IVC filter) Myelodysplastic syndrome and other blood dyscrasias

Design outcomes

Primary

MeasureTime frame
Active factor Xa level. Timepoint: At baseline, 4 hours after the first injection, day 10 of the study 12 hours after the last injection. Method of measurement: The measurement of active factor levels was followed up by the laboratory without the researchers' knowledge of how the test was performed.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoum khoshfetrat

Zahedan University of Medical Sciences

khoshfetrat@zaums.ac.ir+98 915 349 0213

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026