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OpenTrials
Completed

NCT Number: NCT02050438

How Total Knee Prosthesis Dessigns Influence in Quality of Live

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

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Key information

Age range

65 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Corporació Sanitària Parc Taulí

Sabadell, Barcelona, 08208, Spain

About this study

Objectiu Criteris d'inclusió Mesura dels resultats

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Total knee arthroplasty

Procedure

Other names: Total Knee Prostesis

Primary outcomes

  1. Quality of Life

    Time frame: 6 months

Secondary outcomes

  1. Functional Results

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Corporacion Parc Tauli

Other

Registry information

Important dates

Study start
2014
Primary completion
2014
First posted
Jan 30, 2014
Registry last updated
Jul 28, 2014

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.

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