How Total Knee Prosthesis Dessigns Influence in Quality of Live

July 25, 2014 updated by: Jordi Villalba Modol, Corporacion Parc Tauli
The purpose of this study is to determine whether different kind of prostesis designs influences in the quality of life of patients

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Objectiu Criteris d'inclusió Mesura dels resultats

Study Type

Observational

Enrollment (Anticipated)

135

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Spain
    • Barcelona
      • Sabadell, Barcelona, Spain, 08208
        • Corporacio Sanitaria Parc Tauli

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years to 80 years (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients operated Total Knee Arthroplasty 6 months previously the observational study

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Quality of Life
Time Frame: 6 months
6 months

Secondary Outcome Measures

Outcome Measure
Time Frame
Functional Results
Time Frame: 6 months
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Corporacion Parc Tauli

Investigators

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

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Actual)

July 1, 2014

Study Registration Dates

First Submitted

January 29, 2014

First Submitted That Met QC Criteria

January 29, 2014

First Posted (Estimate)

January 30, 2014

Study Record Updates

Last Update Posted (Estimate)

July 28, 2014

Last Update Submitted That Met QC Criteria

July 25, 2014

Last Verified

July 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • COTCSPT1JV

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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