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The SOX Trial: Compression Stockings to Prevent the Post-Thrombotic Syndrome

NCT00143598 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 806

Last updated 2014-08-18

Study results available
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Summary

The purpose of this study is to determine whether elastic compression stockings used for 2 years are effective in preventing the post-thrombotic syndrome in patients with symptomatic proximal deep venous thrombosis.

Conditions

  • Deep Venous Thrombosis

Interventions

DEVICE

Knee-length, graduated elastic compression stocking

Worn daily for 2 years, 30-40 mm Hg

DEVICE

Knee-length, placebo stocking

Worn daily for two years

Sponsors & Collaborators

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV

  • Sigvaris Corporation

    collaborator INDUSTRY

  • Sir Mortimer B. Davis - Jewish General Hospital

    lead OTHER

Principal Investigators

  • Susan R. Kahn, M.D., M.Sc. · Sir Mortimer B. Davis - Jewish General Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-06-30
Primary Completion
2012-02-29
Completion
2012-02-29

Countries

  • United States
  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00143598 on ClinicalTrials.gov