The CUSA Clarity Bone Tip Study

NCT04300075 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2023-08-07

No results posted yet for this study

Summary

The aim of the Study is to investigate the clinical performance and surgeon preferences of the CUSA Clarity Bone Tip during skull base surgery with removal of bony, and other cranial calcified tissue.

Conditions

  • Cranial Skull Base Bone Removal

Interventions

DEVICE

CUSABT

Subject receives use of the CUSA Clarity Bone Tip product during cranial skull base bone removal surgery

Sponsors & Collaborators

  • Integra LifeSciences Corporation

    lead INDUSTRY

Principal Investigators

  • Jason Marzuola · Integra LifeSciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-30
Primary Completion
2024-08-31
Completion
2024-08-31
FDA Device
Yes

Countries

  • Germany
  • Greece
  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04300075 on ClinicalTrials.gov