A Study Utilizing Escitalopram in Glioma Patients

Last updated: June 17, 2025
Sponsor: University of Nebraska
Overall Status: Active - Recruiting

Phase

2

Condition

Cancer

Brain Cancer

Brain Tumor

Treatment

Escitalopram Oral Capsules

Escitalopram Oral Tablet

Clinical Study ID

NCT03728673
0245-18-FB
  • Ages > 19
  • All Genders

Study Summary

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

Inclusion

Inclusion Criteria:

  • 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

  • Life expectancy greater than 6 months

  • Able to provide written informed consent for study participation

  • Negative urine pregnancy test at enrollment for females of childbearing potential

  • Female participants must be either post-menopausal (free from menses for 2 or moreyears), surgically sterilized, or willing to use two adequate barrier forms ofcontraception

Exclusion

Exclusion Criteria:

  • 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

  • Already taking an anti-depressant (SSRI or NSRI)

  • Have problems tolerating past treatment with SSRI or NSRIs

Study Design

Total Participants: 20
Treatment Group(s): 2
Primary Treatment: Escitalopram Oral Capsules
Phase: 2
Study Start date:
March 06, 2019
Estimated Completion Date:
August 31, 2027

Study Description

As many as 85% of patients with glioma, a cancer of glial cells, 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. Commonly, impairments in visuospatial skills and executive function are seen. There is evidence that serotonin selective reuptake inhibitors (SSRIs) such as escitalopram improve modulation and function of resting state networks, contribute to neuroplastic changes in brain regions subserving these abilities, and provide general functional support to neuronal cells. In addition to either improving cognition or preventing cognitive decline, treatment with an SSRI may also improve outcomes critical to overall survival in this vulnerable population, including functional independence, psychosocial stability, and quality of life.

This study will characterize the degree of change in cognition/brain function in participants with grade IV glioma planning to undergo concurrent chemoradiation therapy followed by temozolomide and 17 weeks of treatment with an SSRI, escitalopram, and determine the degree of change in psychosocial function as assessed via ratings in mood and quality of life. The study hypothesis is that following treatment with escitalopram participants will experience improved cognitive and mood function over time.

Connect with a study center

  • University of Nebraska Medical Center

    Omaha, Nebraska 68198
    United States

    Active - Recruiting

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