In order to assess the efficacy of hydroxychloroquine treatment weekly for a total of 7 weeks in the prevention of COVID-19 infection, three hundred sixty (360) Healthcare workers with high risk exposure to patients infected with COVID-19 will be tested for COVID-19 infection via nasopharyngeal (NP) swab once weekly for 7 weeks. Of those, one hundred eighty (180) will receive weekly doses of hydroxychloroquine for the duration of the study. Subjects who opt not to receive the study drug will form the control group.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
221
Weekly treatment in individuals at high risk
Baylor University Medical Center
Dallas, Texas, United States
Number of Participants Infected With COVID-19 or COVID-19 Like Illness During the Trial
Number of participants infected with COVID-19 or identified as having COVID-19 like illness during the trial
Time frame: Up to 7 weeks after study initiation
Time From Study Initiation Until the Occurrence of COVID-19 or COVID-19 Like Illness or Being Censored
Time-to-first clinical event consisting of a persistent change for any of the following: * diagnosis of COVID-19 * clinical characteristics of COVID-19 like illness * being censored
Time frame: Up to 7 weeks after study initiation
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