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NCT05815251

Porous Titanium Microspheres in Kyphoplasty

Status unknown Last updated 21 April 2023
What this trial tests

trial in Vertebral Fracture in 15 participants. Status unknown.

Timeline
1 January 2021
Primary endpoint
31 December 2023
31 December 2024

Quick facts

Lead sponsorUnit of neurosurgery, Departement of Neurosciences, University of Torino
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment15
Start date1 January 2021
Primary completion31 December 2023
Estimated completion31 December 2024
Sites1 location across Italy

Conditions studied

Sponsor

Unit of neurosurgery, Departement of Neurosciences, University of Torino

Who can join

55 and older, any sex, with Vertebral Fracture or Kyphoplasty. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Study is a prospective observational, performed in the context of normal clinical practice, of patients with osteoporotic vertebral compression fractures identified as candidates for kyphoplasty treatment with porous trabecular titanium microspheres (see whether to put commercial name and company). The study does not involve any interference with the patient's diagnostic-therapeutic course The objective of the study is the clinical-radiological evaluation of the efficacy of kyphoplasty treatment with trabecular porous titanium spheres in terms of pain control and reduction of kyphotic deformity following fracture. Further evaluation of the safety of the treatment in terms of absence of intraoperative adverse events and material-related toxicity.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Vertebral Fracture

Currently open trials in the same condition.

Other Unit of neurosurgery, Departement of Neurosciences, University of Torino trials

Trials by the same sponsor.

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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/NCT05815251.

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