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NCT00143598 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study of Deep Venous Thrombosis, sponsored by Sir Mortimer B. Davis - Jewish General Hospital.

Completed
Registry status
Phase 3
Development phase
806
Enrollment target
20
Study locations

NCT00143598: Completed Phase 3 study of Deep Venous Thrombosis, sponsored by Sir Mortimer B. Davis - Jewish General Hospital.

NCT00143598 is a Phase 3 study of Deep Venous Thrombosis that has completed, run by Sir Mortimer B. Davis - Jewish General Hospital. The registered enrollment target is 806 participants, above the 377-participant average among 9 other Deep Venous Thrombosis trials with a reported enrollment target (114% higher). The trial reports 20 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00143598, a Phase 3 study of Deep Venous Thrombosis, has completed, sponsored by Sir Mortimer B. Davis - Jewish General Hospital.

COMPLETED
Registry status
Phase 3
Development phase
806 participants
Enrollment target
20
Study locations

Study 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 Studied

Interventions

  • DEVICE Knee-length, graduated elastic compression stocking
  • DEVICE Knee-length, placebo stocking

Study Locations (20)

Ontario

  • Hamilton Health Sciences - General Hospital - Hamilton
  • Hamilton Health Sciences - Chedoke Division - Hamilton
  • Hamilton Health Sciences - McMaster University Medical Centre - Hamilton
  • St. Joseph's Healthcare Hamilton - Hamilton
  • Hamilton Health Sciences - Henderson General Hospital - Hamilton
  • London Health Sciences Centre - London
  • The Ottawa Hospital, Civic Campus - Ottawa
  • Sunnybrook & Women's College Health Sciences Centre - Toronto
  • University Health Network - Toronto General Hospital - Toronto

Quebec

  • Centre Hospitalier Pierre-Boucher - Longueuil
  • Hôpital Maisonneuve-Rosemont - Montreal
  • Centre Hospitalier de l'Université de Montréal - Hôpital Notre-Dame - Montreal
  • Centre Hospitalier de l'Université de Montréal - Hôpital Hôtel-Dieu - Montreal
  • Royal Victoria Hospital - McGill University Health Centre - Montreal

Michigan

  • Henry Ford Health Systerm - Detroit

North Carolina

  • Duke University Medical Center - Durham

Oklahoma

  • Oklahoma University Health Sciences Center - Oklahoma City

British Columbia

  • Victoria Heart Institute Foundation - Victoria

Manitoba

  • St. Boniface General Hospital - Winnipeg

Nova Scotia

  • QE II Health Sciences Centre - Halifax

Trial Details

FieldValue
Enrollment Target 806 participants
Start Date 2004-06
Est. Completion 2012-02
Phase Phase 3

What the finished NCT00143598 record still lists

NCT00143598 is an interventional study that assigns participants to a tested intervention. The registered 806 participants enrollment target is mid-sized for trials with a published cap, above the 377-participant average among 9 other Deep Venous Thrombosis trials with a reported enrollment target (114% higher).

The record links to 1 condition, with Deep Venous Thrombosis appearing as the primary indexed condition, and to 2 interventions - of which Knee-length, graduated elastic compression stocking is the first listed.

NCT00143598 names 20 study sites across 8 states, led by Ontario, Quebec, Michigan.

Frequently Asked Questions

What is clinical trial NCT00143598 about?

NCT00143598 is a clinical study titled "The SOX Trial: Compression Stockings to Prevent the Post-Thrombotic Syndrome". 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.

What is the current status of trial NCT00143598?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 806 participants. The study started on 2004-06. Estimated completion is 2012-02.

What conditions does trial NCT00143598 study?

This clinical trial studies the following conditions: Deep Venous Thrombosis.

What interventions are being tested in trial NCT00143598?

The interventions under investigation include: Knee-length, graduated elastic compression stocking (DEVICE), Knee-length, placebo stocking (DEVICE).

Who is sponsoring clinical trial NCT00143598?

This trial is sponsored by Sir Mortimer B. Davis - Jewish General Hospital, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00143598 being conducted?

This trial has 20 study locations across Michigan, North Carolina, Oklahoma, British Columbia, Manitoba. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Deep Venous Thrombosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00143598's enrollment target sits among peer trials

806 2nd of 9 the highest of 9 other Deep Venous Thrombosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Deep Venous Thrombosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00143598, the US trial registry maintained by the National Library of Medicine. NCT00143598 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.