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NCT05180071

A Post-market Study Evaluating Clinical and Radiographic Outcomes of Total Elbow Arthroplasty With TEMA

Not yet recruiting NA Last updated 12 December 2023
What this trial tests

NA trial testing TEMA elbow system in Total Elbow Arthroplasty in 59 participants. Not yet recruiting.

Timeline
1 February 2024
Primary endpoint
30 June 2029
30 June 2029

Quick facts

Lead sponsorLimacorporate S.p.a
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment59
Start date1 February 2024
Primary completion30 June 2029
Estimated completion30 June 2029

Drugs / interventions tested

Conditions studied

Sponsor

Limacorporate S.p.a

Who can join

18 and older, any sex, with Total Elbow Arthroplasty. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

TEMA elbow system is a CE marked medical device, and within this clinical trial it is used according to its intended use. This is a Post Marketing Clinical Follow Up trial, with the main aim to collect evidences on the outcome data on this product, by analysing clinical scoring systems, radiographs and adverse event records within five years after the surgery, and thus to assess the short-term performance and safety of this implant.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Limacorporate S.p.a trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05180071.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing