C3 Total Joint Patient Registry

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

UNKNOWN

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-05-31

Brief Summary

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

This study will assess the efficacy of products, implants, and procedures for knee and hip replacement.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

A Study to Evaluate the Conformis iTotal Identity Knee Replacement System

NCT04667559

Osteoarthritis, Knee

TERMINATED

Rejuvenate Modular Outcomes Study

NCT01257568

Arthroplasty, Replacement, Hip

COMPLETED NA

Improving Prosthetic Arms for Amputee: A Better Fit and More Functionality

NCT05990062

Amputation, Surgical

RECRUITING NA

A Clinical Registry of Orthobiologics Procedures

NCT03011398

Orthopedic Disorder

ENROLLING_BY_INVITATION

A Clinical Investigation of the M2a- 38™ Hip System

NCT00698503

Non-inflammatory Degenerative Joint Disease Osteoarthritis Avascular Necrosis

TERMINATED

Detailed Description

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

This registry will prospectively collect a core set of data on patients undergoing knee or hip replacement. This registry will include a variety of different products, implants, technologies and procedures. The registry will also collect any adverse events/complications that occur during or following these surgeries. This database can also be utilized in the future to answer research questions, by retrospectively going back through the data. This information also may go to insurance companies or hospitals for quality measurement and metrics reporting. The data will be utilized to develop strategic treatment pathways that will improve patient care. Ultimately, the goal of the registry is to enhance the understanding of treatment associated with knee and hip replacement and the resulting patient outcomes. The registry will also be used to provide quality measurement and metrics reporting.

Conditions

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

Knee Replacement Hip Replacement

Study Design

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

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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

Knee Replacement

Patients undergoing knee replacement surgery

No interventions assigned to this group

Hip Replacement

Patients undergoing hip replacement

No interventions assigned to this group

Eligibility Criteria

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

Inclusion Criteria

* At least 18 years of age
* Undergoing knee or hip replacement
* Subject is likely to follow standard of care post-operative follow up for at least 1 year

Exclusion Criteria

* Inability to complete follow-up visits or required questionnaires
* Inability to provide informed consent without a legally authorized representative

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No