About this trial

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 criteria

Qualifiers

Adult patients scheduled for endoscopic endonasal skull base surgery

Disqualifiers

Pre-existing anosmia

Patients has a history of previous endoscopic endonasal skull base surgery

Trial design

Treatments tested in this trial

  • Endoscopic endonasal skull base surgery

Treatment groups

No treatment groups listed

Locations

3
Belgium
KU Leuven3000, LeuvenVlaams-Brabant, Belgium
Germany
Max Planck Research Unit for Neurogenetics69, Frankfurt am MainHesse, Germany
Netherlands
Leiden University Medical Center10702, LeidenSouth Holland, Netherlands

Sponsors and collaborators

Universitaire Ziekenhuizen KU Leuven

Lead sponsor