Failed Conservative Radial Head Fracture Treatment Clinical Trial
Official title:
A Focused Registry to Document the Use of the Short- or Long-stemmed Radial Head Prosthesis (RHP)
Verified date | August 2020 |
Source | AO Innovation Translation Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The purpose of this focused registry is to evaluate the clinical implications of the RHP position (relative to the articulations) regarding functional and radiographic parameters in patients treated with the RHP with a straight and curved stem.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | January 2016 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 years or older - Use of a short-or long-stemmed DePuy Synthes Radial Head Prosthesis due to any of the following indications: - Fresh fracture of the radial head which is not amendable to an adequate -steosynthesis - Post-traumatic deformity or arthroses - Failed open reduction internal fixation (ORIF) - Failed conservative radial head fracture treatment - Informed consent obtained, i.e.: - Ability to understand the content of the patient information / Informed Consent Form - Willingness and ability to participate in the clinical investigation according to the Clinical Investigation Plan (CIP) - Signed and dated Ethics Committee (EC) / Institutional Review Board (IRB) approved written informed consent Exclusion Criteria: - Active infection at the affected elbow - Any not medically managed severe systemic disease - Pregnancy - Prisoner - Recent history of substance abuse (ie, recreational drugs, alcohol) that would preclude reliable assessment |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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AO Clinical Investigation and Publishing Documentation |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluation of the functional outcome | Elaborate if there is an association between the implant head and stem position (relative to the elbow articulations), functional outcomes and radiological parameters (radiolucency and arthritis) after 1 year in patients treated with a RHP | 12 Months | |
Secondary | Evaluation of functional outcome | Elaborate if there is an association between the implant head and stem position (relative to the elbow articulations), functional outcomes and radiological parameters (radiolucency and arthritis) after 2 years | 24 months | |
Secondary | Range of motion | To investigate range of motion of the injured limb as compared to the contralateral side | 12 months | |
Secondary | Adverse events | To evaluate if the related adverse events have an effect on quality of life (EQ5D) | 12 months |