Influence of Tourniquet Use and Surgery Duration on the Incidence of Deep Vein Thrombosis in Total Knee Arthroplasty
This study has been completed.
Sponsor:
University of Sao Paulo General Hospital
Information provided by (Responsible Party):
University of Sao Paulo General Hospital
ClinicalTrials.gov Identifier:
NCT01559532
First received: March 13, 2012
Last updated: March 19, 2012
Last verified: March 2012
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Purpose
This is an observational study to analyze the influence of surgery duration and tourniquet time in the incidence of deep venous thrombosis (DVT) in patients that had undergone total knee arthroplasty (TKA).
| Condition |
|---|
|
Deep Vein Thrombosis |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Influence of Tourniquet Use and Surgery Duration on the Incidence of Deep Vein Thrombosis in Total Knee Arthroplasty |
Resource links provided by NLM:
Further study details as provided by University of Sao Paulo General Hospital:
Primary Outcome Measures:
- Deep vein thrombosis [ Time Frame: 7 days ] [ Designated as safety issue: No ]Deep vein thrombosis confirmed by ascending venography performed 7 days after total knee arthroplasty.
| Enrollment: | 78 |
| Study Start Date: | February 2008 |
| Study Completion Date: | September 2011 |
| Primary Completion Date: | June 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
ATK patients
Patients from our institution that underwent cemented TKA for degenerative knee disorders.
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 30 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Seventy-eight consecutive patients from our institution underwent cemented TKA for degenerative knee disorders and then underwent AV, for which they gave informed consent, at a point between 7 and 12 days after surgery, after having been discharged from the hospital.
Criteria
Inclusion Criteria:
- patients that underwent cemented total knee arthroplasty
Exclusion Criteria:
- post-operative infection
- inadequate follow-up
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01559532
Locations
| Brazil | |
| Orthopedics Department - University of Sao Paulo General Hospital | |
| São Paulo, Brazil, 05403-010 | |
Sponsors and Collaborators
University of Sao Paulo General Hospital
Investigators
| Study Director: | Arnaldo J Hernandez, Prof. Dr. | Orthopedics and Traumatology Department - University of Sao Paulo General Hospital |
More Information
Publications:
| Responsible Party: | University of Sao Paulo General Hospital |
| ClinicalTrials.gov Identifier: | NCT01559532 History of Changes |
| Other Study ID Numbers: | 222 |
| Study First Received: | March 13, 2012 |
| Last Updated: | March 19, 2012 |
| Health Authority: | Brazil: Ethics Committee |
Keywords provided by University of Sao Paulo General Hospital:
|
Deep vein thrombosis Thromboembolism Tourniquet Knee prosthesis. |
Additional relevant MeSH terms:
|
Thrombosis Venous Thrombosis Embolism and Thrombosis Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on May 23, 2013