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Osteochondritis Dissecans clinical trials

View clinical trials related to Osteochondritis Dissecans.

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NCT ID: NCT05332288 Recruiting - Clinical trials for Osteochondritis Dissecans Knee

Triphasic Osteochondral Scaffold for the Treatment of the OCD of the Knee: Observational Study

MAIOCD
Start date: April 1, 2022
Phase:
Study type: Observational

The objective of the present study is to evaluate the clinical results of reconstructive treatment of knee OCD defects treated with osteochondral scaffolds implanted with specific instrumentation.The evaluation will be performed through clinical, subjective and objective assessments.

NCT ID: NCT04649905 Recruiting - Clinical trials for Psychological Stress

Psychological Response and Readiness Associated With OCD of the Knee

Start date: January 4, 2021
Phase:
Study type: Observational

This study primarily aims to determine whether patients diagnosed with osteochondritis dissecans (OCD) of the knee experience psychological stress due to their diagnosis and treatment plan. Secondarily, this study aims to determine whether knee OCD patients experience a change in stress and depression as they progress through their standard-of-care treatment plan, and whether they have impaired psychological readiness for return to sport.

NCT ID: NCT04364334 Recruiting - Clinical trials for Osteoarthritis, Knee

Knee Registry (Knieregister)

Start date: January 2017
Phase:
Study type: Observational [Patient Registry]

Rationale: In view of patient care, patient characteristics and treatment parameters are registered for all patients visiting the Mobility Clinic of the University Medical Center Utrecht for orthopaedic knee treatment. Patients also fill out questionnaires for function, pain and mobility of the knee, before and after treatment. Objective: The main objective of this registry is to collect patient characteristics and treatment parameters together with data from the questionnaires in a database. This knee registry can be used for future research questions. Study design: This is a longitudinal observational registry. Study population: All patients that visit the Mobility Clinic will be asked to participate in the knee registry. Patients that meet one or more of the following criteria will be excluded: are below the age of 16, not able or willing to sign the broad consent form, not being able to read and understand Dutch language, or receiving medical treatment for their knee elsewhere. Main study parameters/endpoints: Data will be collected for future research for which the purpose is not known at this time. When new research will be conducted, study parameters will be set. A study application has to be submitted to the institutional ethical review board of the University Medical Center Utrecht. Patients do not need to be asked permission for the use of their data for each study individually. Only when additional information is needed. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The burden for patients to participate in this registry is minimal and consists of time. Any future results may be beneficial for patients. Participation or refusal to participate in the registry has no consequences for their treatment.

NCT ID: NCT04297449 Completed - Clinical trials for Osteochondritis Dissecans

Prospective 2-year Data Collection of the First 10 Patients After Ankle Spacer Implantation

Start date: January 18, 2019
Phase:
Study type: Observational

Osteochondral defects (OCD) of the talus are pathologic lesions of the talar cartilage and its subchondral bone and might severely deteriorate the quality of life. For the treatment of multiple and/or large talar OCDs and in patients with failed previous surgical treatment the Ankle Spacer was developed. Six patients are included in a prospective clinical and radiological study with a follow-up of two years.

NCT ID: NCT03656185 Active, not recruiting - Clinical trials for Osteochondritis Dissecans

Elbow Arthroscopy Data Analysis

EA
Start date: March 15, 2018
Phase:
Study type: Observational

The purpose of this study is to evaluate preoperative objective measurements and operative objective measurements to determine if there is any effect to postoperative outcomes. Patients who were 13 years old or greater at the time of arthroscopic osteocapsular release were followed clinically and radiographically to determine best practice and optimal treatment and technique, risk and rate of complication, and postoperative outcomes.

NCT ID: NCT03588975 Recruiting - Clinical trials for Articular Cartilage Disorder of Knee

A Study of MACI in Patients Aged 10 to 17 Years With Symptomatic Chondral or Osteochondral Defects of the Knee

PEAK
Start date: October 24, 2018
Phase: Phase 3
Study type: Interventional

The objective of this study is to compare the efficacy and safety of MACI® vs arthroscopic microfracture in the treatment of patients aged 10 to 17 years with symptomatic articular chondral or osteochondral defects of the knee.

NCT ID: NCT03452098 Completed - Clinical trials for Osteochondritis Dissecans

Post-Operative Rehabilitation of Knee Osteochondral Defect: A Case Series

Start date: January 2011
Phase:
Study type: Observational

A case-series review was performed on five collegiate athletes with osteochondral lesions of the knee at California State University, Northridge (CSUN). All subjects received surgical intervention to treat the defect. The surgeries performed were either an Osteoarticular Transfer System (OATS) procedure and/or a Microfracturing procedure. Subjects were treated post-operatively by the CSUN team physical therapist and/or athletic trainers at CSUN. This paper seeks to provide information about osteochondral defects of the knee, the surgical interventions, and a protocol for post-operative treatment and rehabilitation of such injuries.

NCT ID: NCT03190200 Completed - Clinical trials for OCD - Osteochondritis Dissecans

MRI Findings of Epiphyseal Growth Plate in Healthy Children

Start date: January 1, 2018
Phase:
Study type: Observational

The purpose of the study is to determine if by using MRI changes can be identified changes early on in the knees of young children that may be at risk for developing osteochondritis dissecans. If MRI can identify changes then better council can be offered about the risks of future activity and treatment options.

NCT ID: NCT02993510 Completed - Cartilage Injury Clinical Trials

A Randomized Controlled Trial Comparing Chondro-Gide® to Microfracture Alone for Treatment of Knee Cartilage Defects.

Start date: December 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of using Chondro-Gide® collagen membrane either sutured or glued compared to microfracture alone in the treatment of symptomatic cartilage defects of the knee.

NCT ID: NCT02771496 Active, not recruiting - Clinical trials for Osteochondritis Dissecans

Osteochondritis Dissecans of Knee Prospective Cohort

Start date: May 2014
Phase:
Study type: Observational

The Cohort is a multi-site prospective data collection study that will enroll any patient with diagnosis of knee OCD (confirmed by a standard of care x-ray or MRI). Patients will be followed for up to the next 50 years of their lives to study courses of care, disease progression, treatment/surgical options/results, and specific sports-related outcomes in athletic patients. Subjects will complete quality of life surveys as part of the Cohort. Course of care will not be affected.