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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01488175
Other study ID # H-2-2011-100
Secondary ID
Status Withdrawn
Phase Phase 4
First received December 2, 2011
Last updated March 17, 2015
Start date January 2012
Est. completion date January 2015

Study information

Verified date March 2015
Source Hvidovre University Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection AgencyDenmark: National Board of HealthDenmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if the use of a tourniquet during insertion of a cemented primary total knee arthroplasty will influence clinical and radiological (measured with RSA X-ray technique) outcome.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- clinical diagnosis og osteoarthritis of the knee

- patients must be 18 years or older

- patients must understand and speak danish

- must be able to give signed consent

Exclusion Criteria:

- severe medical illness

- documented osteoporosis

- rheumatoid arthritis

- prior surgery in the knee

- neuropathy

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
tourniquet
a tourniquet around the thigh is used during insertion of the TKA to achieve a bloodless environment
no tourniquet
a tourniquet around the thigh is not used during insertion of the TKA

Locations

Country Name City State
Denmark Dept. of Orthopedics, University Hospital of Hvidovre, Denmark. Hvidovre

Sponsors (1)

Lead Sponsor Collaborator
Hvidovre University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary migration of the prosthesis in millimeters assessed vith RSA. does the use of a tourniquet around the thigh during insertion of a primary TKA affect postoperative migration of the prosthesis? 2 years No
Secondary postoperative pain. Does the use of a tourniquet affect postoperative pain, patient satisfaciton and knee range of motion 2 years No
Secondary Patient satisfaction (VAS-scale) Does the use of a tourniquet affect postoperative pain, patient satisfaciton and knee range of motion 2 years No
Secondary Knee range of motion (degrees) Does the use of a tourniquet affect postoperative pain, patient satisfaciton and knee range of motion 2 years No
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