Cognitive Status After Removal of Skull Base Meningioma

Part of paid clinical trials in Columbus, Ohio.

Sponsor
Ohio State University
Study ID
NCT04635657
Status
Recruiting
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Conditions

  • Cognitive Decline
  • Cognitive Impairment
  • Frontal Meningioma
  • Meningioma
  • Post-Surgical Cognition
  • Skull Base Meningioma
  • Temporal Meningioma

Eligibility Criteria

Sex
ALL
Age
18 Years - 89 Years
Healthy Volunteers
Not accepted

Interventions

  • Long-term Cognitive testing — OTHER
    These patients will undergo their standard of care cognitive testing at baseline, six weeks post-operatively and one year post-operatively.

Study Details

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.

Key Dates

Start date
Dec 10, 2019
Status verified
May 2026
Primary completion
Dec 31, 2027
Completion
Dec 31, 2028

Study Design

Enrollment
50 participants (estimated)

Arms

  • Arm: 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

Primary Outcome Measure

Overall cognitive function [ Time Frame: 12 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Ohio State University Wexner Medical CenterColumbusOhio43210
Emma Kurtz, BS
[email protected]
(614) 685-4534
Uchechi Okafor, BS
[email protected]
614-293-4876
Daniel Prevdello, MD (PRINCIPAL_INVESTIGATOR)

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By research site
Ohio State University Wexner Medical Center· Columbus, OH

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