Pre and Post-Operative Cognitive Status in Patients Undergoing Surgery for Resection of Meningioma Associated With the Frontal and Temporal Lobes

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 89
View:

• 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.

Locations
United States
Ohio
Ohio State University Wexner Medical Center
RECRUITING
Columbus
Contact Information
Primary
Megan Frost, BS
Megan.Frost@osumc.edu
614-685-8622
Backup
Uchechi Okafor, BS
Uchechi.Okafor@osumc.edu
614-293-4876
Time Frame
Start Date: 2019-12-10
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 50
Treatments
Meningioma Group
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
Related Therapeutic Areas
Sponsors
Leads: Ohio State University

This content was sourced from clinicaltrials.gov