New Tool of Subjective and Objective Functional Evaluation and the Quality of Life After Arthroplastic Surgery of the Hip and the Knee Assisted or Not by Computer and Mini-invasive Arthroplasty

NCT ID: NCT00894218

Last Updated: 2014-02-25

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

TERMINATED

Clinical Phase

NA

Total Enrollment

1 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-04-30

Study Completion Date

2010-04-30

Brief Summary

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

Hip or knee arthroplasties allow a relief of pain and a good functional habilitative at patients suffering from degenerative osteoarthritis of these articulations with medium and long-term good results. The main objective of this study is to compare the efficiency in short and medium-term functional impact parlance of two surgical techniques: computer-assisted surgery and mini-invasive surgery compared to the conventional techniques thanks to an innovative technology of ambulatory analysis of walking.

Detailed Description

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

Conditions

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

Hip Arthritis Knee Arthritis

Study Design

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

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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

Conventional arthroplasty

Total hip or knee conventional arthroplasty

Group Type ACTIVE_COMPARATOR

Arthroplasty

Intervention Type PROCEDURE

Hip or knee arthroplasty

Mini-invasive arthroplasty

Total hip or knee mini-invasive arthroplasty

Group Type EXPERIMENTAL

Arthroplasty

Intervention Type PROCEDURE

Hip or knee arthroplasty

Mini-invasive and computer-assisted arthroplasty

Mini-invasive and computer-assisted total hip or knee arthroplasty

Group Type EXPERIMENTAL

Arthroplasty

Intervention Type PROCEDURE

Hip or knee arthroplasty

Interventions

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

Arthroplasty

Hip or knee arthroplasty

Intervention Type PROCEDURE

Eligibility Criteria

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

Inclusion Criteria

* Weight \< 100 kg
* score UCLA \> 4
* prosthesis of first intention

Exclusion Criteria

* Pregnant
* score UCLA \< 4
* osteotomy near to prosthesis
* prosthesis requiring an osseous transplant
* prosthesis already set up
* infections, contagious diseases (HIV, tuberculosis, hepatitis, venereal diseases) or metastasis
* neuromuscular diseases able to perturb walking or staying
* congenital or acquired disease, or previous surgery able to have consequences on results and prosthesis survey according to the surgeon
Minimum Eligible Age

20 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.

Assistance Publique Hopitaux De Marseille

OTHER

Sponsor Role lead

Responsible Party

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

Responsibility Role SPONSOR

Locations

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

Assistance Publique-Hopitaux de Marseille

Marseille, , France

Site Status

Countries

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

France

Other Identifiers

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

2007-A0084845

Identifier Type: -

Identifier Source: secondary_id

2007-26

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Balance After Knee Arthroplasty
NCT04681404 UNKNOWN NA