Home › Meningioma › NCT04635657
Cognitive Status After Removal of Skull Base Meningioma
RecruitingObservational study
Pre and Post-Operative Cognitive Status in Patients Undergoing Surgery for Resection of Meningioma Associated With the Frontal and Temporal Lobes
Who can join
Ages 18 to 89 · All sexes
Full eligibility criteria
Inclusion Criteria: * Subject has a meningioma associated with the frontal or temporal lobes * Subject is scheduled to undergo open craniotomy or Endoscopic Endonasal surgery * Subject is 18 years of age or older * 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 * Previous surgery will not exclude the patient as a new baseline cognitive evaluation will occur. Exclusion Criteria: * Patient is a prisoner * Patient is 90 years of age or older * Pregnant women * Previous radiation to the brain
About the study
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.
What is being tested
- Long-term Cognitive testing (other)
Sponsor: Ohio State University · Participants: 50 · Started: Dec 10, 2019
Contact the study team
- Emma Kurtz, BS · Phone: (614) 685-4534
- Uchechi Okafor, BS · Phone: 614-293-4876
Official record on ClinicalTrials.gov — NCT04635657
Locations in the U.S.
| Ohio | Ohio State University Wexner Medical Center, Columbus |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.