Clinical Trials Logo

Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01615692
Other study ID # MOP-102610
Secondary ID ISRCTN71334751;
Status Withdrawn
Phase
First received June 1, 2012
Last updated April 16, 2018
Start date June 2004
Est. completion date June 2015

Study information

Verified date April 2018
Source Sir Mortimer B. Davis - Jewish General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate leg health for one additional year in patients with symptomatic proximal deep venous thrombosis who did not already develop Post-Thrombotic Syndrome (PTS) during the 2 years of follow up in the SOX Trial.


Description:

The post-thrombotic syndrome (PTS) is a frequent, burdensome and costly condition that occurs in about one third of patients after an episode of deep vein thrombosis (DVT). Affected patients have chronic leg pain and swelling, and sometimes develop skin ulcers. At present, there is little to offer for the treatment of this condition. Prevention of PTS is the key to reducing its burden on patients and society. Elastic compression stockings (ECS) for two years following DVT could be helpful in preventing or delaying onset of PTS at three years, however data supporting this is limited.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Consecutive patients with a first, symptomatic, objectively confirmed proximal DVT diagnosed within the last 14 days (with or without concurrent distal DVT or pulmonary embolism)

- Who have no contraindications to standard treatment with heparin and/or warfarin, and

- Who provide informed consent to participate

Exclusion Criteria:

- Contraindication to compression stockings

- Limited lifespan (estimated < 6 months)

- Geographic inaccessibility preventing return for follow-up visits

- Inability to apply stockings daily and unavailability of a caregiver to apply stockings daily

- Treatment of acute DVT with thrombolytic agents

Study Design


Locations

Country Name City State
Canada QE II Health Sciences Centre Halifax Nova Scotia
Canada Hamilton Health Sciences - Chedoke Division Hamilton Ontario
Canada Hamilton Health Sciences - General Hospital Hamilton Ontario
Canada Hamilton Health Sciences - Henderson General Hospital Hamilton Ontario
Canada Hamilton Health Sciences - McMaster University Medical Centre Hamilton Ontario
Canada St. Joseph's Healthcare Hamilton Hamilton Ontario
Canada London Health Sciences Centre London Ontario
Canada Centre Hospitalier de l'Université de Montréal - Hôpital Notre-Dame Montreal Quebec
Canada Hôpital du Sacré-Coeur de Montréal Montreal Quebec
Canada Hôpital Maisonneuve-Rosemont Montreal Quebec
Canada Montreal General Hospital - McGill University Health Centre Montreal Quebec
Canada Royal Victoria Hospital - McGill University Health Centre Montreal Quebec
Canada Sir Mortimer B. Davis - Jewish General Hospital Montreal Quebec
Canada St. Mary's Hospital Centre Montreal Quebec
Canada The Ottawa Hospital, Civic Campus Ottawa Ontario
Canada Centre hospitalier affilié universitaire de Québec, Hôpital de l'Enfant-Jésus Quebec City Quebec
Canada Sunnybrook & Women's College Health Sciences Centre Toronto Ontario
Canada University Health Network Toronto Ontario
Canada Victoria Heart Institute Foundation Victoria British Columbia
Canada St. Boniface General Hospital Winnipeg Manitoba

Sponsors (4)

Lead Sponsor Collaborator
Sir Mortimer B. Davis - Jewish General Hospital Canadian Institutes of Health Research (CIHR), Heart and Stroke Foundation of Canada, Sigvaris Corporation

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Kahn SR, Shbaklo H, Shapiro S, Wells PS, Kovacs MJ, Rodger MA, Anderson DR, Ginsberg JS, Johri M, Tagalakis V; SOX Trial Investigators. Effectiveness of compression stockings to prevent the post-thrombotic syndrome (the SOX Trial and Bio-SOX biomarker substudy): a randomized controlled trial. BMC Cardiovasc Disord. 2007 Jul 24;7:21. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of PTS and PTS severity 3 year follow up
See also
  Status Clinical Trial Phase
Recruiting NCT05003843 - BOLT: Study of the Indigo® Aspiration System When Used in Patients With Deep Vein Thrombosis N/A
Recruiting NCT03937947 - Traumatic Brain Injury Associated Radiological DVT Incidence and Significance Study
Withdrawn NCT04136561 - Novel Strategy to Encourage Early Removal of Central Venous Catheters N/A
Completed NCT03420625 - Blood Flow Stimulation in the Lower Limbs by Application of Different External Devices N/A
Recruiting NCT02507180 - Safely Ruling Out Deep Vein Thrombosis in Pregnancy With the LEFt Clinical Decision Rule and D-Dimer
Completed NCT02555111 - Xarelto Versus no Treatment for the Prevention of Recurrent Thrombosis in Patients With Chronic Portal Vein Thrombosis. Phase 3
Completed NCT01975090 - The SENTRY Clinical Study N/A
Terminated NCT02469376 - Evaluation of a New Imagingtechnologie for Thrombosis Phase 1
Completed NCT02037607 - Incidence of Venous Thromboembolism in Children Undergoing Elective Neurosurgical Procedures N/A
Not yet recruiting NCT01357941 - Need for Antepartum Thromboprophylaxis in Pregnant Women With One Prior Episode of Venous Thromboembolism (VTE) N/A
Completed NCT00773448 - Screening for Occult Malignancy in Patients With Idiopathic Venous Thromboembolism N/A
Completed NCT00720915 - D-dimer to Select Patients With First Unprovoked Venous Thromboembolism Who Can Have Anticoagulants Stopped at 3 Months N/A
Completed NCT00771303 - Ruling Out Pulmonary Embolism During Pregnancy:a Multicenter Outcome Study
Completed NCT00244725 - Odiparcil For The Prevention Of Venous Thromboembolism Phase 2
Completed NCT00264277 - D-dimer to Establish Duration of Anticoagulation After Venous Thromboembolism Phase 4
Completed NCT00365950 - 3 Months' Versus 6 Months' Anticoagulation in Patients With DVT and/or PE Phase 4
Completed NCT00182403 - Fixed Dose Heparin Study Phase 3
Completed NCT03682419 - Evaluation of Precision and Accuracy of INR Measurements in a Point of Care Device (OPTIMAL) N/A
Not yet recruiting NCT04981327 - The API-CALF Study: Apixaban to Treat Calf Vein Thrombosis Phase 3
Recruiting NCT03240120 - A Study of Dabigatran Etexilate as Primary Treatment of Malignancy Associated Venous Thromboembolism Phase 3