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Post-traumatic Arthritis clinical trials

View clinical trials related to Post-traumatic Arthritis.

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NCT ID: NCT05719935 Recruiting - Osteoarthritis Clinical Trials

The KinematX Midcarpal Total Wrist Arthroplasty Registry

Start date: April 26, 2021
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to learn about functional and patient reported outcomes in patient undergoing total wrist replacement with the KinematX total wrist replacement study. The main questions it aims to answer are: - What is the range of motion (flexion, extension, radial, ulnar, grip and pinch strength) at 3-, 6-, and 12-months after surgery and yearly up to 10 years among patients having total wrist replacement with the KinematX implant. - What are the patient reported outcomes (PROMIS, PRWE, HSS wrist expectations) at 3-, 6-, and 12-months after surgery and yearly up to 10 years among patients having total wrist replacement with the KinematX implant. - How do range of motion and patient reported outcomes change over the 10 years after total wrist replacement surgery? Participants will be followed according to standard of care and preoperative and post-operative information for up to 10 years after surgery will be collected and entered into an electronic data base. Patients are eligible to enroll into the registry before or after they have had their wrist replacement surgery.

NCT ID: NCT05197036 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory Arthritis

Start date: December 21, 2021
Phase:
Study type: Observational

A clinical trial investigating the safety and effectiveness of Smith and Nephew's FDA-approved Porous Total Knee System, which is used to replace worn away and diseased knee joints. The aim of this study is to show that most patients who receive the Porous Total Knee System have reduced pain, greater mobility and a long-lasting implant post-surgery.

NCT ID: NCT04191733 Terminated - Clinical trials for Rheumatoid Arthritis

Anterior Advantage With KINCISE

Start date: January 28, 2020
Phase: N/A
Study type: Interventional

This is a post-market prospective, 1:1 randomized, multicenter non-inferiority study to compare the femoral broaching time for THA with the Anterior Advantage approach with KINCISE vs. without KINCISE. Follow-up will continue through 24 weeks post-op.

NCT ID: NCT03726554 Active, not recruiting - Clinical trials for Post-Traumatic Arthritis

Post-Market Study of Comprehensive Reverse Augmented Glenoid and Mini Humeral Tray in Total Shoulder Arthroplasty

Start date: August 28, 2018
Phase: N/A
Study type: Interventional

This study is a multicenter, prospective, non-randomized, non-controlled, dual cohort post market surveillance study. The primary objective of this study is to confirm the safety and performance of the Comprehensive Reverse Shoulder System when used with the Comprehensive Porous Augmented Glenoid Baseplate and/or Comprehensive Mini Humeral Tray in primary and revision reverse shoulder arthroplasty.

NCT ID: NCT03626038 Recruiting - Clinical trials for Rheumatoid Arthritis

Post Market Clinical Follow-up (PMCF) Study of the A.L.P.S. Proximal Humerus Plating System

Start date: June 19, 2018
Phase: N/A
Study type: Interventional

This study is a multicenter, prospective, non-randomized, non-controlled post-market clinical follow-up study. The primary objective of this study is to confirm the safety and performance of the A.L.P.S. Proximal Humerus Plating System applied in proximal humerus fracture treatment.

NCT ID: NCT03542045 Completed - Osteoarthritis Clinical Trials

China ATTUNE® Study

Start date: April 12, 2018
Phase:
Study type: Observational [Patient Registry]

The study was designed as prospective, single-arm, multi-center which was intended to broadly capture all patients as the technology is adopted.

NCT ID: NCT03357445 Active, not recruiting - Clinical trials for Post-Traumatic Arthritis

AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study

Start date: October 14, 2011
Phase: N/A
Study type: Interventional

This is a Post Marketing Clinical Follow Up study (PMCF) on the AVANTAGE RELOAD dual mobility system cup.

NCT ID: NCT03343171 Active, not recruiting - Osteoarthritis Clinical Trials

Continuum Ceramic on Ceramic Bearing Post Market Clinical Follow-Up Study

Start date: September 15, 2010
Phase:
Study type: Observational

The primary objective of this study is to obtain implant survivorship and clinical outcome data for the commercially available Zimmer® Continuum™ Ceramic-on-Ceramic Bearing System when used in primary hip arthroplasty. This will be done by analysis of standard scoring systems, radiographs and adverse event records. Data will be used to monitor pain, mobility and survivorship, and to confirm the safety and efficacy of the Continuum Ceramic-on-Ceramic Bearing System.

NCT ID: NCT03168672 Active, not recruiting - Osteoarthritis Clinical Trials

GLOBAL ICON Stemless Shoulder System Post Market Clinical Follow Up Study

Global ICON
Start date: October 18, 2017
Phase: N/A
Study type: Interventional

This is a Post Market Clinical Follow Up (PMCF) study to monitor the safety and performance of the GLOBAL ICON stemless humeral component. The data gathered will be used to support post market surveillance of the device, and may potentially be used for additional market access purposes.

NCT ID: NCT03142958 Suspended - Clinical trials for Rheumatoid Arthritis

Clinical Evaluation of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement (CADENCE)

Cadence
Start date: August 24, 2017
Phase: N/A
Study type: Interventional

A post market, prospective, non-randomized, multi-center, open-label,clinical study using survivorship as the reference performance goal to study the safety and efficacy of the Cadence Total Ankle System (TAS) when used for primary ankle arthroplasty.