[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100411294":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":23,"locations":33,"responsibleParty":53,"collaborators":10,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":10,"eligibilityCriteria":62,"healthyVolunteers":58,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":10,"studyType":69,"phases":10,"briefSummary":70,"conditions":71,"keywords":10,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"Ohio State University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Meningioma Group",null,"This group will include all patients in the study, regardless of location (frontal or temporal lobe) or surgical approach (endoscopic endonasal or craniotomy). Fifty patients will be included in the cohort",[13],"Other: Long-term Cognitive testing",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"Long-term Cognitive testing","These patients will undergo their standard of care cognitive testing at baseline, six weeks post-operatively and one year post-operatively.",[9],[20],{"name":21,"affiliation":5,"role":22},"Daniel Prevedello, MD","PRINCIPAL_INVESTIGATOR",[24,29],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"Emma Kurtz, BS","CONTACT","(614) 685-4534","Emma.Kurtz@osumc.edu",{"name":30,"role":26,"phone":31,"phoneExt":10,"email":32},"Uchechi Okafor, BS","614-293-4876","Uchechi.Okafor@osumc.edu",[34],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Ohio State University Wexner Medical Center","RECRUITING","Columbus","Ohio","43210","United States","US",{"type":43,"coordinates":44},"Point",[45,46],-82.99879,39.96118,{"lat":46,"lon":45},[49,50,51],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},{"name":30,"role":26,"phone":31,"phoneExt":10,"email":32},{"name":52,"role":22,"phone":10,"phoneExt":10,"email":10},"Daniel Prevdello, MD",{"type":22,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Daniel M. Prevedello","Clinical Professor","100411294","cognitive-status-after-removal-of-skull-base-meningioma-100411294",false,"NCT04635657","Cognitive Status After Removal of Skull Base Meningioma","Pre and Post-Operative Cognitive Status in Patients Undergoing Surgery for Resection of Meningioma Associated With the Frontal and Temporal Lobes","Inclusion Criteria:\n\n* Subject has a meningioma associated with the frontal or temporal lobes\n* Subject is scheduled to undergo open craniotomy or Endoscopic Endonasal surgery\n* Subject is 18 years of age or older\n* The subject must in the investigator's opinion, be psychosocially, mentally, and physically able to fully comply with this protocol including the required follow-up visits, the filling out of required forms, and have the ability to understand and give written informed consent\n* Previous surgery will not exclude the patient as a new baseline cognitive evaluation will occur.\n\nExclusion Criteria:\n\n* Patient is a prisoner\n* Patient is 90 years of age or older\n* Pregnant women\n* Previous radiation to the brain","ALL","18 Years","89 Years",{"count":67,"type":68},50,"ESTIMATED","OBSERVATIONAL","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.",[72,73,74,75,76,77,78],"Meningioma","Skull Base Meningioma","Frontal Meningioma","Temporal Meningioma","Cognitive Impairment","Cognitive Decline","Post-Surgical Cognition","2026-05-19",{"date":81,"type":82},"2026-05-22","ACTUAL",{"date":84,"type":82},"2019-12-10",{"date":86,"type":68},"2028-12-31",{"name":5,"class":6},1]