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Evaluation of the Enoxaparin in the Prophylaxis of Deep Venous Thrombosis

Evaluation of the Two Different Enoxaparin Regimen in the Prophylaxis of Deep Venous Thrombosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130917014693N11
Enrollment
60
Registered
2020-05-18
Start date
2018-07-23
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Deep vein thrombosi. Other venous embolism and thrombosis

Interventions

Intervention 1: Control group: Patients receive pre-filled syringes of enoxaparin (manufactured by Alborz Daroo company) at dose of 40 mg/day through subcutaneous route. Intervention 2: Intervention g

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age between 18 and 65 years old Padua risk score = 4 points Signing the informed consent form

Exclusion criteria

Exclusion criteria: Patients in shock state Acute kidney injury Chronic kidney injury History of hemorrhage in past one month Invasive surgical procedures which needs to enoxaparin discontinuation Pregnancy Lactation Thrombophilia Antithrombin deficiency Previous history of venous thrombosis Body mass index more than 35 kg/m2 Platelet less than 50000 cells/uL

Design outcomes

Primary

MeasureTime frame
The activity level of anti factor Xa. Timepoint: Three hours after third doses. Method of measurement: Chromogenic assay.

Secondary

MeasureTime frame
Occurance rate of deep vein thrombosis. Timepoint: Daily. Method of measurement: Clinical examination and sonography is necessary cases.;Occurrence rate of adverse drug reactions. Timepoint: Daily. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Sahraei

Shahid Beheshti University of Medical Sciences

zahra.sahraei@yahoo.com+98 21 5541 9005

Outcome results

None listed

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