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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.
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
| Field | Value |
|---|---|
| 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.
Learn More About Clinical Trials
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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.
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