Clinical Outcomes Study of the Nexel Total Elbow - Join Clinical Trial NCTNCT02469662
How to Join This Clinical Trial - NCTNCT02469662
Learn how to participate in this NA trial studying an investigational therapy for Elbow Joint Destruction, Post-traumatic Lesions, Ankylosed Joints, Advanced Rheumatoid Arthritis, Joint Instability or Loss of Motion, Acute Comminuted Articular Fracture of Elbow Joint Surfaces, Bone Loss Contributing to Elbow Instability, Bilateral Ankylosis From Causes Other Than Active Sepsis, Post-traumatic Arthritis, Degenerative Arthritis. This study is currently enrolling participants.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Elbow Joint Destruction, Post-traumatic Lesions, Ankylosed Joints, Advanced Rheumatoid Arthritis, Joint Instability or Loss of Motion, Acute Comminuted Articular Fracture of Elbow Joint Surfaces, Bone Loss Contributing to Elbow Instability, Bilateral Ankylosis From Causes Other Than Active Sepsis, Post-traumatic Arthritis, Degenerative Arthritis. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
- Elbow Joint Destruction, Post-traumatic Lesions, Ankylosed Joints, Advanced Rheumatoid Arthritis, Joint Instability or Loss of Motion, Acute Comminuted Articular Fracture of Elbow Joint Surfaces, Bone Loss Contributing to Elbow Instability, Bilateral Ankylosis From Causes Other Than Active Sepsis, Post-traumatic Arthritis, Degenerative Arthritis
- Treatment Being Tested
- Investigational treatment
- Study Phase
- NA - Research study
- Enrollment Status
- Currently enrolling participants
- Study Identifier
- NCTNCT02469662 - ClinicalTrials.gov Identifier
- Sponsored By
- Study sponsor
What to Expect as a Participant
Participating in this clinical trial involves:
- Initial screening to determine eligibility
- Regular study visits and health assessments
- Receiving the study treatment or placebo
- Medical monitoring and follow-up care
- Contributing to medical research that may help others
- Potential access to new treatments before they're widely available
Clinical Trial Benefits and Compensation
Participants in this clinical research study may receive:
- Close medical monitoring by healthcare professionals
- Access to potential new treatments
- Compensation for time and travel (varies by study)
- No-cost study-related medical care
- The opportunity to help advance medical knowledge
Where Is This Clinical Trial Located?
This study is enrolling participants at 11 locations. Find a study site near you:
Clinical Research Site
Golden, Colorado 80401 - United States
Status: RECRUITING
Clinical Research Site
Charlotte, North Carolina 28207 - United States
Status: RECRUITING
Clinical Research Site
Philadelphia, Pennsylvania 19107 - United States
Status: RECRUITING
Clinical Research Site
Germantown, Tennessee 38138 - United States
Status: RECRUITING
Clinical Research Site
Sydney, New South Wales 2067 - Australia
Status: TERMINATED
Clinical Research Site
Tampere, - Finland
Status: RECRUITING
Clinical Research Site
Toulouse, - France
Status: TERMINATED
Clinical Research Site
Pforzheim, - Germany
Status: TERMINATED
Clinical Research Site
Torino, 10128 - Italy
Status: RECRUITING
Clinical Research Site
Breda, - Netherlands
Status: ACTIVE_NOT_RECRUITING
And 1 more locations available. Contact us to find the nearest participating site.
How to Enroll in This Study
To learn more about participating in this NA clinical trial for Elbow Joint Destruction, Post-traumatic Lesions, Ankylosed Joints, Advanced Rheumatoid Arthritis, Joint Instability or Loss of Motion, Acute Comminuted Articular Fracture of Elbow Joint Surfaces, Bone Loss Contributing to Elbow Instability, Bilateral Ankylosis From Causes Other Than Active Sepsis, Post-traumatic Arthritis, Degenerative Arthritis:
- Review the eligibility criteria with your healthcare provider
- Contact the study team for a pre-screening interview
- Schedule an in-person screening visit if eligible
- Review and sign the informed consent form
- Begin participation in the clinical trial
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