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Clinical Trials/ISRCTN10903007
ISRCTN10903007
Completed
未知

Treatment of benign bone lesions with an injectable biphasic bone substitute

Medical University of Vienna0 sites18 target enrollmentJuly 21, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Benign bone lesions
Sponsor
Medical University of Vienna
Enrollment
18
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 21, 2022
End Date
March 27, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients who:
  • 1\. Received treatment with a ceramic biphasic bone substitute
  • 2\. For benign bone tumors and tumor\-like lesions
  • 3\. With a complete set of retrospective information, including surgical protocols, X\-rays, patient dismission letters and outpatient clinic protocols
  • 4\. With a minimum follow\-up of 1 year after surgery

Exclusion Criteria

  • 1\. Inconclusive data with missing surgical or histological reports

Outcomes

Primary Outcomes

Not specified

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