Multicenter Registry for Effectiveness Analysis of ActiveCare+S.F.T® Mobile Compression Device for Thrombosis Prevention in Hip and Knee Arthroplasty
Public ClinicalTrials.gov record NCT01984190. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
ActiveCare+S.F.T® Outcomes Registry (ACOR)
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Venous thromboembolic events (VTE), either deep vein thromboses or pulmonary emboli, are important complications in patients undergoing knee or hip arthroplasty. This multicenter Clinical Registry is aimed at collecting large volume clinical effectiveness data of ActiveCare+S.F.T® mobile compression device +/- aspirin in lowering the potential risk of venous thromboembolism (VTE) prophylaxis in patients undergoing primary lower extremity total joint arthroplasty. The results can then be compared to pharmacology protocols.
Study identification
- NCT ID
- NCT01984190
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 411 participants
Conditions and interventions
Conditions
Interventions
Not listed
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Mar 31, 2011
- Primary completion
- Sep 30, 2011
- Completion
- Sep 30, 2011
- Last update posted
- Sep 3, 2014
2011
United States locations
- U.S. sites
- 10
- U.S. states
- 9
- U.S. cities
- 10
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Arkansas Specialty Orthopaedics | Little Rock | Alaska | 72205 | — |
| Shiley Center for Orthopaedic Research and Education at Scripps Clinic | La Jolla | California | 92037 | — |
| VA Palo Alto Health Care System | Menlo Park | California | 94025 | — |
| Rubin Institute for Advanced Orthopedics, | Baltimore | Maryland | 21215 | — |
| Twin Cities Orthopaedics | Edina | Minnesota | 55435 | — |
| Washington University School of Medicine, Department of Orthopaedic Surgery | St Louis | Missouri | 63310 | — |
| Hospital for Special Surgery | New York | New York | 10021 | — |
| Cleveland Clinic | Cleveland | Ohio | 44195 | — |
| The Center Orthopedic & Neurosurgical Care &Research | Bend | Oregon | 97710 | — |
| Anderson Orthopaedic Clinic | Alexandria | Virginia | 22306 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01984190, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Sep 3, 2014 · Synced Sep 2, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01984190 live on ClinicalTrials.gov.