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Study identifier: NCT03728673 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study Utilizing Escitalopram in Glioma Patients

Condition: Glioma of Brain · Glioma  ·  Sponsor: University of Nebraska

PhasePhase 2
Planned participants20
Who can joinAll sexes, 19 Years to no upper limit
Healthy volunteersNo

About this study

Glioma is a cancer of glial cells, a class of tissue supporting neuronal function in the brain. As many as 85% of glioma patients experience cognitive impairment. This is not only from direct tumor involvement, but also from therapy such as cranial radiation and chemotherapy, which degrades neuronal function. There is evidence that serotonin selective reuptake inhibitors (SSRIs), such as escitalopram, improve cognition or prevent cognitive decline and may also improve outcomes critical to overall survival including functional independence, psychosocial stability, and quality of life. This pilot study will evaluate the effectiveness of the selective serotonin reuptake inhibitor (SSRI) escitalopram for treating cognitive impairment in newly diagnosed grade IV glioma over a 17 week treatment period.

This description comes directly from the study's public registry record.

Talk to the study team

Michaela K Savine, RN  ·  402-836-9488  ·  misavine@unmc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Nebraska Medical CenterOmaha, Nebraska, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT03728673