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Completed No phase listed Observational

Multicenter Registry for Effectiveness Analysis of ActiveCare+S.F.T® Mobile Compression Device for Thrombosis Prevention in Hip and Knee Arthroplasty

ClinicalTrials.gov ID: NCT01984190

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.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 10:10 PM EDT

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
Lead sponsor
Medical Compression Systems
Industry
Enrollment
411 participants

Conditions and interventions

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
Apr 2011 (Type not available)
Primary completion
Oct 2011 (Actual)
Completion
Oct 2011 (Actual)
Last update posted
Sep 4, 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 4, 2014 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01984190 live on ClinicalTrials.gov.

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