Endoscopic endonasal skull base surgery: This intervention will be performed as part of the standard-of-care for patients scheduled for endoscopic endonasal skull base surgery for lesions in the (para)sellar region
Study summary
In this study, the research team will investigate the incidence and etiology of olfactory dysfunction following endoscopic endonasal skull base surgery, by combining clinical assessments with histomolecular analysis.
Eligibility
Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria:
* Adult patients scheduled for endoscopic endonasal skull base surgery
Exclusion Criteria:
* Pre-existing anosmia
* Patients has a history of previous endoscopic endonasal skull base surgery
Primary outcome measure(s)
Incidence of olfactory dysfunction — From enrollment to the last evaluation 6 months postoperatively
Incidence of trigeminal dysfunction — From enrollment to the last evaluation 6 months postoperatively
Etiology of olfactory and trigeminal dysfunction following endoscopic endonasal skull base surgery — Until the end of study (at 3 years)
Trial sites (3)
Facility
City
Region
Status
KU Leuven
Leuven
Vlaams-Brabant
Recruiting
Max Planck Research Unit for Neurogenetics
Frankfurt am Main
Hesse
Active Not Recruiting
Leiden University Medical Center
Leiden
South Holland
Not Yet Recruiting
More Universitaire Ziekenhuizen KU Leuven trials in Germany
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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