search
Back to results

Doppler Ultrasound Following Unicondylar Knee Replacement to Determine the Incidence of Postoperative DVT

Primary Purpose

Number of Deep Venous Thrombosis (DVT)

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Doppler Ultrasound
Sponsored by
Hospital for Special Surgery, New York
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Number of Deep Venous Thrombosis (DVT) focused on measuring DVT

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Hospital for Special Surgery

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

DVT

Arm Description

Doppler Ultrasound

Outcomes

Primary Outcome Measures

Deep venous thrombosis

Secondary Outcome Measures

body mass index

Full Information

First Posted
May 23, 2014
Last Updated
March 20, 2017
Sponsor
Hospital for Special Surgery, New York
search

1. Study Identification

Unique Protocol Identification Number
NCT02148757
Brief Title
Doppler Ultrasound Following Unicondylar Knee Replacement to Determine the Incidence of Postoperative DVT
Official Title
Doppler Ultrasound Following Unicondylar Knee Replacement to Determine the Incidence of Postoperative DVT
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital for Special Surgery, New York

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Purpose of this study is to determine the incidence of deep venous thrombosis after partial knee replacement.
Detailed Description
Doppler Ultrasound will be performed 2-6 weeks after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Number of Deep Venous Thrombosis (DVT)
Keywords
DVT

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DVT
Arm Type
Other
Arm Description
Doppler Ultrasound
Intervention Type
Procedure
Intervention Name(s)
Doppler Ultrasound
Primary Outcome Measure Information:
Title
Deep venous thrombosis
Time Frame
2-6 weeks after surgery
Secondary Outcome Measure Information:
Title
body mass index
Time Frame
at date of surgery

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Hospital for Special Surgery
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Doppler Ultrasound Following Unicondylar Knee Replacement to Determine the Incidence of Postoperative DVT

We'll reach out to this number within 24 hrs