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Image guided endoscopic sinus surgery

Conditions
paranasal sinus malignancy, sinus cancer
Registration Number
NL-OMON20396
Lead Sponsor
AV
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
Not specified
Target Recruitment
6
Inclusion Criteria

•Primary tumours of the paranasal sinus (T1-T4a for non-melanomas and T3-T4a for melanomas), confirmed by biopsy. Recurrent cases are also eligible.

•Any lymph node status

Exclusion Criteria

•Unresectable tumours of the paranasal sinus

•Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The main parameter of this pilot study is the technical success of implementing CBCT during endoscopic sinus surgery as an additional tool for the control of the resection. Operating time will be recorded and the mean duration of the procedure will be calculated. Assessment of the possible residual tumour volume will be also performed based on the intraoperative CBCT, as well as comparison to the planned resection volume as calculated in the preoperative imaging planning. The quality of CBCT and MRI scan matching will also be evaluated. No correlation to clinicopathological parameters will be established in this study.
Secondary Outcome Measures
NameTimeMethod
ot applicable
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