Spots Global Cancer Trial Database for Cognitive Status After Removal of Skull Base Meningioma
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Trial Identification
Brief Title: Cognitive Status After Removal of Skull Base Meningioma
Official Title: Pre and Post-Operative Cognitive Status in Patients Undergoing Surgery for Resection of Meningioma Associated With the Frontal and Temporal Lobes
Study ID: NCT04635657
Interventions
Study Description
Brief Summary: The purpose of this prospectively enrolling trial is to assess long-term cognitive outcomes of patients undergoing surgery for resection of a meningioma associated with the frontal and temporal lobes.
Detailed Description: This study will look at patients who are undergoing resection of a skull based meningioma, located in the frontal or temporal lobe, via craniotomy or via endoscopic endonasal approach. The study will compare cognitive function at baseline, at six weeks postoperatively and at one year postoperatively. The cognitive testing being done at baseline will be a clinical care set of assessments done by the speech language pathology team and will include the RBANS tests, the MoCA, PROMIS-29, and NeuroQOL-Cognitive Functions.
Keywords
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
Ohio State University Wexner Medical Center, Columbus, Ohio, United States
Contact Details
Name: Daniel Prevedello, MD
Affiliation: Ohio State University Wexner Medical Center
Role: PRINCIPAL_INVESTIGATOR
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