RECRUITING

Cognitive Status After Removal of Skull Base Meningioma

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2019-12-10
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04635657

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Subject has a meningioma associated with the frontal or temporal lobes
  2. * Subject is scheduled to undergo open craniotomy or Endoscopic Endonasal surgery
  3. * Subject is 18 years of age or older
  4. * 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
  5. * Previous surgery will not exclude the patient as a new baseline cognitive evaluation will occur.
  1. * Patient is a prisoner
  2. * Patient is 90 years of age or older
  3. * Pregnant women
  4. * Previous radiation to the brain

Contacts and Locations

Study Contact

Megan Frost, BS
CONTACT
614-685-8622
Megan.Frost@osumc.edu
Uchechi Okafor, BS
CONTACT
614-293-4876
Uchechi.Okafor@osumc.edu

Principal Investigator

Daniel Prevedello, MD
PRINCIPAL_INVESTIGATOR
Ohio State University Wexner Medical Center

Study Locations (Sites)

Ohio State University Wexner Medical Center
Columbus, Ohio, 43210
United States

Collaborators and Investigators

Sponsor: Ohio State University

  • Daniel Prevedello, MD, PRINCIPAL_INVESTIGATOR, Ohio State University Wexner Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-12-10
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2019-12-10
Study Completion Date2024-12-31

Terms related to this study

Additional Relevant MeSH Terms

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