Fluoxetine to Reduce Hospitalization From COVID-19 Infection (FloR COVID-19)
Withdrawn before enrolling · Early Phase 1 · Has a placebo group
Conditions studied: Covid19
In brief
The current research is a pilot study to determine the feasibility of recruiting and retaining 40 participants diagnosed with COVID-19. The purpose is to observe the early use of fluoxetine (commonly known as Prozac) to reduce the severity of the COVID-19 illness. Fluoxetine is a drug that has been approved by the U.S. Food and Drug Administration (FDA) since 1987 for various mental health disorders.
Key facts
- Study ID
- NCT04570449
- Run by
- Milton S. Hershey Medical Center
- People needed
- 0
- Starts
- 2020-11-01
- Expected to finish
- 2021-12-01
- Last updated by the study team
- 2020-12-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- English speaking participant
- 18 years of age or older
- able to give informed consent
- Tested positive for active SARS-CoV-2 infection and
- It's been less than 10 days since symptoms first appeared;
- Fever persists for longer than 24 hours without the use of fever reducing medications; and
- Experiencing other symptoms of COVID-19 as described by the CDC
You may not qualify if…
- Prisoner or institutionalized patient
- Unable to give informed consent
- Less than 18 years of age
- Hospitalization
- Active bleeding requiring blood products in past week
- Diagnosed with bipolar disorder and not on mood stabilizing medication
- Known allergy or hypersensitivity to fluoxetine
- Currently taking a monoamine oxidase inhibitor (MAOI)
- Currently taking an selective serotonin reuptake inhibitor (SSRI) or selective norepinephrine reuptake inhibitor (SNRI)
- Outpatient and currently taking hydroxychloroquine
- Known pregnancy
- Breastfeeding
- Known prolonged QTc, such as congenital prolonged QTc syndromes
Where it is running
- Milton S. Hershey Medical Center Clinical Research Center — Hershey, Pennsylvania, United States
Full record on ClinicalTrials.gov
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