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Looking for participantsPhase4

THRomboprophylaxis in Individuals Undergoing Superficial endoVEnous Treatment (THRIVE)

Sponsor: Imperial College London

NCT ID: NCT05735639

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Dalteparin Sodium (drug), Tinzaparin Sodium (drug), Enoxaparin Sodium (drug), Rivaroxaban (drug)
How long the study runs
Study runs about 47 months (dates as stated)
About the drug or intervention
Dalteparin Sodium — drug: Low molecular weight heparin · Tinzaparin Sodium — drug: Low molecular weight heparin · Enoxaparin Sodium — drug: Low molecular weight heparin · Rivaroxaban — drug: Direct oral anticoagulant · Apixaban — drug: Direct oral anticoagulant · Dabigatran Etexilate — drug: Direct oral anticoagulant
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
3,175
Started
2024-01-22
Last checked
2026-06

Plain English Summary

What is this study?

  • • Testing a new treatment for venous thromboembolism
  • • Phase4 - 3,175 participants
  • • Endovenous interventions are keyhole operations for varicose veins that are carried out from within the vein itself

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with venous thromboembolism

Where?

  • • London - Imperial College Hospital NHS Foundation Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Endovenous interventions are keyhole operations for varicose veins that are carried out from within the vein itself. Varicose veins are enlarged veins close to the surface of the skin. They are connected to the bigger deeper veins in the leg (known as deep veins). Because of this, operations to close the varicose veins can increase the chance of a blood clot forming in the deep veins. Blood clots in the deep veins happen in around 1 in 50 people after endovenous operations. A clot in the leg can cause swelling, pain, and other long-term problems. If a clot in the leg breaks off and travels to the lungs, it can cause problems with the lung' ability to move oxygen from the air into the blood and may, in rare cases, be life threatening. Varicose vein procedures may carry a slightly higher risk of blood clot formation, and we are currently unsure if current clot reducing medicines are beneficial in preventing blood clots in people having varicose vein procedures. This study will investigate if it is worthwhile prescribing medicines to reduce blood clots after varicose vein procedures.

Venous ThromboembolismVaricose Veins

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Biomarkers mentioned

have a positive

What the study is looking for

  • ✓Adults (\>18 years)
  • ✓Scheduled to undergo endovenous intervention of truncal varicose veins under local anaesthesia
  • ✓Treatment technologies including radiofrequency, laser, mechanochemical, foam sclerotherapy and cyanoacrylate glue

Who cannot take part

  • ✗Clinical indication for therapeutic anticoagulation e.g., atrial fibrillation
  • ✗Previous personal or first-degree relative history of VTE
  • ✗Thrombophilia
  • ✗Female patients of childbearing potential who have a positive pregnancy test
  • ✗A history of allergy to heparins or direct oral anticoagulants
See the full criteria
Inclusion Criteria: * Adults (\>18 years) * Scheduled to undergo endovenous intervention of truncal varicose veins under local anaesthesia * Treatment technologies including radiofrequency, laser, mechanochemical, foam sclerotherapy and cyanoacrylate glue Exclusion Criteria: * Clinical indication for therapeutic anticoagulation e.g., atrial fibrillation * Previous personal or first-degree relative history of VTE * Thrombophilia * Female patients of childbearing potential who have a positive pregnancy test * A history of allergy to heparins or direct oral anticoagulants * A history of heparin-induced thrombocytopenia * Inherited and acquired bleeding disorders * Evidence of active bleeding * Concomitant major health problems such as active cancer and chronic renal and/or liver impairment * Known thrombocytopenia (platelets known to be less than 50 x 109 /l) * Surgery or major trauma in the previous 90 days * Recent ischemic stroke in the previous 90 days * Inability to provide consent

Where Is This Study? (1 UK site)

Imperial College Hospital NHS Foundation Trust

London W6 8RF, United Kingdom

Recruiting
Hospital R&D contact (matched)

Donna Copeland

donna.copeland@nhs.net---

How to Get in Touch

Sarah Whittley

Sponsor contact

CONTACT

+442033117309 s.whittley@imperial.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-06