Clinical Trials Directory

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UnknownNCT04635657

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

Status
Unknown
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Ohio State University · Academic / Other
Sex
All
Age
18 Years – 89 Years
Healthy volunteers

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.

Conditions

Interventions

TypeNameDescription
OTHERLong-term Cognitive testingThese patients will undergo their standard of care cognitive testing at baseline, six weeks post-operatively and one year post-operatively.

Timeline

Start date
2019-12-10
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2020-11-19
Last updated
2023-10-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04635657. Inclusion in this directory is not an endorsement.