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NCT03806881

Long Term Follow-up After Primary or Revision Shoulder Arthroplasty With a Patient- Specific Glenius Implant

ENROLLING BY INVITATION Last updated 13 March 2024
What this trial tests

trial testing reversed glenoid prothesis in Arthroplasty, Replacement, Shoulder in 24 participants. Enrolling by invitation.

Timeline
1 July 2019
Primary endpoint
1 October 2024
1 December 2028

Quick facts

Lead sponsorMaterialise
StatusENROLLING BY INVITATION
Study typeOBSERVATIONAL
Enrollment24
Start date1 July 2019
Primary completion1 October 2024
Estimated completion1 December 2028
Sites4 locations across Belgium, Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Materialise

Who can join

18 and older, any sex, with Arthroplasty, Replacement, Shoulder or Glenoid Cavity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This post-market follow-up study investigates improvement in clinical and radiological outcome after reversed total shoulder arthroplasty with the patient-specific Glenius Glenoid Reconstruction system

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Arthroplasty, Replacement, Shoulder

Currently open trials in the same condition.

Other Materialise 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/NCT03806881.

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