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Deciding the duration of blood thinners following acute venous thromboembolism (VTE) by assessing residual venous thrombosis by ultrasound scan

Optimizing duration of anticoagulation following acute venous thromboembolism (VTE) by assessing residual venous thrombosis by ultrasound – a multicenter randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053767
Enrollment
440
Registered
2023-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: I829- Embolism and thrombosis of unspecified vein

Interventions

Intervention1: Multicenter Randomized controlled trial: Consecutive adult patients with symptomatic DVT with or without associated Pulmonary embolism fulfilling inclusion criteria will be eligible to

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults >18 years diagnosed with acute lower limb DVT with or without associated pulmonary embolism

Exclusion criteria

Exclusion criteria: 1.Previous VTE 2.Any indication for lifelong anticoagulation 3.Contraindications for anticoagulation 4.Active malignancy 5.Pregnancy

Design outcomes

Primary

MeasureTime frame
1.Recurrent VTE 2.Major bleedingTimepoint: 1.30 months from randomization. 2.30 months from randomization.

Secondary

MeasureTime frame
Sensitivity and specificity of PoCUS compared to formal venous scanning for detection of residual venous thrombosisTimepoint: 30 Months

Countries

India

Contacts

Public ContactDr Aneesh Basheer

Dr Moopens Medical College, Wayanad

basheeraneesh@gmail.com9677154338

Outcome results

None listed

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