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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.
The incidence of olfactory dysfunction following endoscopic endonasal skull base surgery remains unclear in current research, and the results vary widely. Additionally, the pathophysiology of this postoperative olfactory dysfunction and the impact of this surgery on the trigeminal system has not been investigated to date. In this study, the investigators developed a state-of-the-art clinical pipeline with olfactory and trigeminal assessments, prior to and following endoscopic endonasal skull base surgery. Furthermore, the investigators will collect surgical waste tissue from the posterior septal mucosa, which is removed during this procedure to gain access to the sphenoid sinus and the (para)sellar region. By performing histomolecular analysis, the research group aims to elucidate the pathophysiology of olfactory dysfunction following this surgery.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Endoscopic endonasal skull base surgery | Procedure | 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 |
|
| Measure | Description | Time Frame |
|---|---|---|
| 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) |
| Measure | Description | Time Frame |
|---|---|---|
| Risk factors for olfactory dysfunction following endoscopic endonasal skull base surgery | Parameters such as smoking history, allergies, age, gender, co-morbidities will be investigated as possible covariates | From enrollment to the last evaluation 6 months postoperatively |
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Inclusion Criteria:
Exclusion Criteria:
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All patients presenting with an indication for endoscopic endonasal skull base surgery for lesions in the anterior skull base (the parasellar region)
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Julie van Waterschoot | Contact | +32477910294 | julie.vanwaterschoot@kuleuven.be |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| KU Leuven | Recruiting | Leuven | Vlaams-Brabant | 3000 | Belgium |
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| ID | Term |
|---|---|
| D008579 | Meningioma |
| D010900 | Pituitary Diseases |
| D010911 | Pituitary Neoplasms |
| D003397 | Craniopharyngioma |
| ID | Term |
|---|---|
| D009380 | Neoplasms, Nerve Tissue |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D009383 | Neoplasms, Vascular Tissue |
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Mucosa of the posterior part of the septum
| Max Planck Research Unit for Neurogenetics | Active, not recruiting | Frankfurt am Main | Hesse | 69 | Germany |
| Leiden University Medical Center | Not yet recruiting | Leiden | South Holland | 10702 | Netherlands |
|
| D008577 | Meningeal Neoplasms |
| D016543 | Central Nervous System Neoplasms |
| D009423 | Nervous System Neoplasms |
| D009371 | Neoplasms by Site |
| D009422 | Nervous System Diseases |
| D007027 | Hypothalamic Diseases |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D004700 | Endocrine System Diseases |
| D004701 | Endocrine Gland Neoplasms |
| D007029 | Hypothalamic Neoplasms |
| D015173 | Supratentorial Neoplasms |
| D001932 | Brain Neoplasms |
| D017599 | Neuroectodermal Tumors |
| D009373 | Neoplasms, Germ Cell and Embryonal |