Hospital for Special Surgery
New York, 10021, United States
Completed
NCT Number: NCT02148757
Doppler Ultrasound Following Unicondylar Knee Replacement to Determine the Incidence of Postoperative DVT
Purpose of this study is to determine the incidence of deep venous thrombosis after partial knee replacement.
Completed
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
About this study
Doppler Ultrasound will be performed 2-6 weeks after surgery.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Unilateral partial knee replacement
- Postoperative anticoagulation with aspirin 325 twice daily
- Regional anesthesia
- Inflatable garments worn during hospitalization
Exclusion criteria
-Bilateral partial knee replacement
Treatment and study plan
Doppler ultrasound
ProcedurePrimary outcomes
-
Deep venous thrombosis
Time frame: 2-6 weeks after surgery
Secondary outcomes
-
body mass index
Time frame: at date of surgery
Sponsors and collaborators
Lead sponsor
Hospital for Special Surgery, New York
Other
Registry information
Important dates
- Study start
- 2011
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- May 28, 2014
- Registry last updated
- Mar 21, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.