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NCT06924567: MULTICIMA

Radiographic Stability of Hip Prosthesis Prior to Revision Surgery

Not yet recruiting Last updated 12 March 2026
What this trial tests

trial testing Implant motion provocation CT in Loosening, Prosthesis in 600 participants. Not yet recruiting.

Timeline
15 September 2026
Primary endpoint
31 December 2029
31 December 2029

Quick facts

Lead sponsorGeorgios Tsikandylakis, MD PhD
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment600
Start date15 September 2026
Primary completion31 December 2029
Estimated completion31 December 2029
Sites6 locations across Denmark, Sweden, Norway

Drugs / interventions tested

Conditions studied

Sponsor

Georgios Tsikandylakis, MD PhD

Who can join

Eligibility, any sex, with Loosening, Prosthesis or Hip Arthropathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this validation study is to compare the preoperative implant stability, assessed by Implant Movement Analysis (IMA), provocation dual CT scans, with the intraoperative stability evaluation in revision hip arthoplasty. The main question it aims to answer is: Does IMA reflect the intraoperative clinical evaluation of implant stability? Participants scheduled for revision hip arthoplasty will undergo IMA preoperativelly in addition to rutine clinical work up. During revision arthoplasty, a surgeon blinded to the IMA results will assess clinically the stability of the hip prosthesis. IMA will be compared with the intraoperative findings to assess IMAs sensitivity and specificity

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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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/NCT06924567.

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