Olfactory Function Following Endoscopic Endonasal Skull Base Surgery
- Conditions
- Skull Base Pathology
- Registration Number
- NCT02165969
- Lead Sponsor
- Ricardo L. Carrau, MD
- Brief Summary
The purpose of this study is to compare a subject's sense of smell before and after endoscopic endonasal surgery to remove a skull base abnormality (i.e. tumor, inflammatory process, fracture, defect, etc.) and use the information collected to validate approaches to surgery that will minimize side effects to the sense of smell function. Data will be collected using a smell identification test along with two questionnaires. In addition, demographic, medical history, treatment, outcome, and follow-up information will be collected.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 160
- Patients presenting with skull base pathologies requiring endonasal surgery at The Ohio State University Wexner Medical Center
- 18 years or older
- Able to consent for self
- Negative serum pregnancy test for women of childbearing potential
- Patient unable to return to clinic at specific follow-up times
- Pregnant or nursing
- Prisoners
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Number of patients with decreased olfactory function after endoscopic endonasal surgery up to 12 months post surgery The subject will complete 2 questionnaires and the University of Pennsylvania Smell Identification Test (UPSIT) at baseline (pre-surgery) and at 1, 3, 6, and 12, months post surgery to determine if the sense of smell has been altered from surgery.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
The Ohio State University
🇺🇸Columbus, Ohio, United States
The Ohio State University🇺🇸Columbus, Ohio, United StatesAmanda McGill, MSContact614-685-8622Amanda.McGill@osumc.eduRicardo Carrau, MDPrincipal Investigator