How Total Knee Prosthesis Dessigns Influence in Quality of Live

Sponsor
Corporacion Parc Tauli (Other)
Overall Status
Completed
CT.gov ID
NCT02050438
Collaborator
(none)
135
1

Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether different kind of prostesis designs influences in the quality of life of patients

Condition or Disease Intervention/Treatment Phase
  • Procedure: Total Knee Arthroplasty

Detailed Description

Objectiu Criteris d'inclusió Mesura dels resultats

Study Design

Study Type:
Observational
Anticipated Enrollment :
135 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Study Start Date :
Jan 1, 2014
Actual Primary Completion Date :
Jul 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Knee Osteoarthritis patients with prostesis treatment

Patients operated previously of Knee Osteoarthritis with different prostesis designs according the Hospital guide

Procedure: Total Knee Arthroplasty
Other Names:
  • Total Knee Prostesis
  • Outcome Measures

    Primary Outcome Measures

    1. Quality of Life [6 months]

    Secondary Outcome Measures

    1. Functional Results [6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Aged 65-80 years.

    • Primary Ostheortritis

    • Mechanical Axis 0+/- 7 degrees

    Exclusion Criteria:
    • Patients with any new important disease after the surgical procedure.

    • Important complications related with the surgical procedure, as fractures, infections and vascular lesions.

    • Patients not following a rehabilitation program

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Corporació Sanitària Parc Taulí Sabadell Barcelona Spain 08208

    Sponsors and Collaborators

    • Corporacion Parc Tauli

    Investigators

    • Principal Investigator: Jordi Villaba-Modol, MD, Corporacio Sanitaria Parc Tauli

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jordi Villalba Modol, Medical Doctor, Corporacion Parc Tauli
    ClinicalTrials.gov Identifier:
    NCT02050438
    Other Study ID Numbers:
    • COTCSPT1JV
    First Posted:
    Jan 30, 2014
    Last Update Posted:
    Jul 28, 2014
    Last Verified:
    Jul 1, 2014
    Keywords provided by Jordi Villalba Modol, Medical Doctor, Corporacion Parc Tauli
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 28, 2014