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Two Weeks of Low Molecular Weight Heparin for Distal Vein Thrombosis (TWISTER)

Primary Purpose

Venous Thrombosis, Pulmonary Embolism

Status
Unknown status
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Enoxaparin
Sponsored by
Monash Medical Centre
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Venous Thrombosis focused on measuring Distal Vein Thrombosis, Proximal Vein Thrombosis, Pulmonary Embolism, Post-thrombotic syndrome, Limited duration treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged 18 years or older with acute symptomatic provoked or unprovoked distal vein thrombosis (axial or muscular veins but not involving trifurcation or distal popliteal vein)
  • Absence of symptomatic pulmonary embolism

Exclusion Criteria:

  • DVT involving trifurcation or more proximal leg veins on imaging
  • Prior DVT
  • Active malignancy ie present at time of diagnosis, or on treatment, or treatment completed within 3 months
  • Ongoing risk factors for propagation e.g. immobility (>50% of day in bed or ≥72 hours), plaster cast or non-weight bearing
  • Other indication for therapeutic anticoagulation (e.g. AF)
  • Active gastro-oesophageal ulceration or bleeding
  • Other high risk for bleeding (e.g. recent neurosurgery, vascular retinopathy, coagulopathy)
  • Platelet count <80 x 109/L
  • Renal impairment (CrCl <30ml/min) • Pregnancy or lactation

Sites / Locations

  • Prince of Wales Hospital
  • Royal Adelaide Hospital
  • Monash Medical Centre, Southern HealthRecruiting
  • Christchurch Hospital

Outcomes

Primary Outcome Measures

Symptomatic recurrence of venous thrombosis (DVT, non fatal and fatal pulmonary embolism) within 3 months.

Secondary Outcome Measures

Asymptomatic proximal thrombus extension at 2 weeks
Time course of symptom resolution and the proportion of patients with complete resolution at two weeks.
Time course of symptom resolution including time to complete resolution of symptoms, and the proportion of patients with complete resolution at two weeks.
All-cause mortality
Post-thrombotic syndrome
Predictors of recurrent or progressive DVT or new PE

Full Information

First Posted
July 20, 2010
Last Updated
December 3, 2010
Sponsor
Monash Medical Centre
Collaborators
Southern Health, Victoria, Eastern Health, Victoria, Royal Adelaide Hospital, Adelaide, Prince of Wales Hospital, Sydney, Christchurch Hospital, NZ, Auckland City Hospital, North Shore Hospital, New Zealand, Middlemore Hospital, New Zealand
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1. Study Identification

Unique Protocol Identification Number
NCT01252420
Brief Title
Two Weeks of Low Molecular Weight Heparin for Distal Vein Thrombosis
Acronym
TWISTER
Official Title
Two Weeks of Low Molecular Weight Heparin for Distal Vein Thrombosis (TWISTER)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2010
Overall Recruitment Status
Unknown status
Study Start Date
November 2010 (undefined)
Primary Completion Date
November 2013 (Anticipated)
Study Completion Date
November 2014 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Monash Medical Centre
Collaborators
Southern Health, Victoria, Eastern Health, Victoria, Royal Adelaide Hospital, Adelaide, Prince of Wales Hospital, Sydney, Christchurch Hospital, NZ, Auckland City Hospital, North Shore Hospital, New Zealand, Middlemore Hospital, New Zealand

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether a limited duration of treatment (two weeks of low molecular weight treatment) is a safe and effective treatment for distal deep vein thrombosis of the lower limb.
Detailed Description
Approximately 50% of symptomatic episodes of deep vein thrombosis (DVT) will be confined to the calf veins (distal DVT). The proportion of distal DVT that propagate to the proximal veins, increasing the risk of pulmonary embolism, is not known. The best treatment of isolated distal DVT is therefore controversial and options include no treatment, follow-up scanning and treatment of only those patients with thrombus propagating to proximal veins, and full anticoagulation for periods ranging from 2 weeks to 3 months. There is good evidence that the 3-month thromboembolic risk in patients with a negative CUS that is limited to the proximal veins is low, in the order of 1%. Previous studies have demonstrated that patients treated with a short period of anticoagulation (4-6 weeks) have a low risk of developing recurrent DVT or PE. In addition, the specificity of CUS for distal DVT is lower than that for proximal DVT, increasing the proportion of false positive findings, making it likely that a proportion of patients diagnosed with distal DVT are treated unnecessarily, with the attendant risks of major and fatal haemorrhage. The need for anticoagulation of patients with distal DVT to prevent recurrent DVT is therefore uncertain, however a survey of current practice suggested that most patients with this condition currently receive antithrombotic therapy. The impact of anticoagulation on initial patient symptoms, and the subsequent risk of the post-thrombotic syndrome are also unclear, and may be a possible alternative justification for antithrombotic therapy. In this proposed multicentre, prospective, cohort study, we plan to determine if a shorter duration of anticoagulation (minimum 2 weeks) is a safe and effective treatment for isolated distal vein thrombosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Thrombosis, Pulmonary Embolism
Keywords
Distal Vein Thrombosis, Proximal Vein Thrombosis, Pulmonary Embolism, Post-thrombotic syndrome, Limited duration treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
330 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Enoxaparin
Other Intervention Name(s)
Clexane
Intervention Description
1.5mg/kg daily for 2 weeks
Primary Outcome Measure Information:
Title
Symptomatic recurrence of venous thrombosis (DVT, non fatal and fatal pulmonary embolism) within 3 months.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Asymptomatic proximal thrombus extension at 2 weeks
Time Frame
2 weeks
Title
Time course of symptom resolution and the proportion of patients with complete resolution at two weeks.
Description
Time course of symptom resolution including time to complete resolution of symptoms, and the proportion of patients with complete resolution at two weeks.
Time Frame
2 weeks
Title
All-cause mortality
Time Frame
3 months
Title
Post-thrombotic syndrome
Time Frame
6 months
Title
Predictors of recurrent or progressive DVT or new PE
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 18 years or older with acute symptomatic provoked or unprovoked distal vein thrombosis (axial or muscular veins but not involving trifurcation or distal popliteal vein) Absence of symptomatic pulmonary embolism Exclusion Criteria: DVT involving trifurcation or more proximal leg veins on imaging Prior DVT Active malignancy ie present at time of diagnosis, or on treatment, or treatment completed within 3 months Ongoing risk factors for propagation e.g. immobility (>50% of day in bed or ≥72 hours), plaster cast or non-weight bearing Other indication for therapeutic anticoagulation (e.g. AF) Active gastro-oesophageal ulceration or bleeding Other high risk for bleeding (e.g. recent neurosurgery, vascular retinopathy, coagulopathy) Platelet count <80 x 109/L Renal impairment (CrCl <30ml/min) • Pregnancy or lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huyen Tran, MBBs(Hons), MClin Epidem
Organizational Affiliation
Monash Medical Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Sydney
State/Province
New South Wales
ZIP/Postal Code
2031
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tim Brighton, MBBs, MD
Phone
+61293829013
Email
Tim.Brighton@SESIAHS.HEALTH.NSW.GOV.AU
First Name & Middle Initial & Last Name & Degree
Tim Brighton, MBBs, MD
Facility Name
Royal Adelaide Hospital
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5000
Country
Australia
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Simon McRae, MBBs, BMedSci
Phone
+61 448882279
First Name & Middle Initial & Last Name & Degree
Simon McRae, MBBs, BMedSci
Facility Name
Monash Medical Centre, Southern Health
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3168
Country
Australia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eileen Merriman, MBChB
Phone
+61 450011998
Email
eileen.merriman@southernhealth.org.au
First Name & Middle Initial & Last Name & Degree
Huyen Tran, MBBS, BClinEpi
Phone
+61 408780785
Email
huyen.tran@southernhealth.org.au
First Name & Middle Initial & Last Name & Degree
Huyen Tran, MBBs, MClinEp
First Name & Middle Initial & Last Name & Degree
Eileen Merriman, MBChB
First Name & Middle Initial & Last Name & Degree
Sanjeev Chunilal, MBChB
Facility Name
Christchurch Hospital
City
Christchurch
State/Province
Canterbury
ZIP/Postal Code
8011
Country
New Zealand
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Smith, MBChB
Phone
+64 3 3640640
Email
mark.smith@cdhb.govt.nz
First Name & Middle Initial & Last Name & Degree
Mark Smith, MBChB

12. IPD Sharing Statement

Citations:
PubMed Identifier
34530387
Citation
Merriman E, Chunilal S, Brighton T, Chen V, McRae S, Ockelford P, Curnow J, Tran H, Chong B, Smith M, Royle G, Crowther H, Slocombe A, Tran H. Two Weeks of Low Molecular Weight Heparin for Isolated Symptomatic Distal Vein Thrombosis (TWISTER study). Thromb Res. 2021 Sep 11;207:33-39. doi: 10.1016/j.thromres.2021.09.004. Online ahead of print.
Results Reference
derived

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Two Weeks of Low Molecular Weight Heparin for Distal Vein Thrombosis

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