How Total Knee Prosthesis Dessigns Influence in Quality of Live

NCT ID: NCT02050438

Last Updated: 2014-07-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

135 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Objectiu Criteris d'inclusió Mesura dels resultats

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteoarthritis Knee Total Knee Replacement

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Knee Osteoarthritis patients with prostesis treatment

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

Total Knee Arthroplasty

Intervention Type PROCEDURE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Total Knee Arthroplasty

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Total Knee Prostesis

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

65 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Corporacion Parc Tauli

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Jordi Villalba Modol

Medical Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jordi Villaba-Modol, MD

Role: PRINCIPAL_INVESTIGATOR

Corporacio Sanitaria Parc Tauli

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Corporació Sanitària Parc Taulí

Sabadell, Barcelona, Spain

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Spain

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

COTCSPT1JV

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

The personalKNEE Trial
NCT06507046 RECRUITING NA