A Study Utilizing Escitalopram in Glioma Patients

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age19+
SponsorUniversity of Nebraska

About this trial

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.

Eligibility criteria

Qualifiers

Pathologically proven diagnosis of Grade IV glioma

Newly diagnosed disease to receive chemotherapy and/or radiation

Performance status Eastern Cooperative Oncology Group (ECOG) 0-2 or equivalent

19 years of age or older

Disqualifiers

Hemifield defects (obscures visual field necessary to participate in all tests)

Inability to undergo MRI

Severe renal impairment defined as Glomerular Filtration Rate (GFR) <30 mL/minute

Screen positive for depression or anxiety

Trial design

Treatments tested in this trial

  • Escitalopram Oral Capsules

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators