Prevention of SARS-CoV-2 in Hospital Workers s Exposed to the Virus (PREP-COVID)
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ClinicalTrials.gov Identifier: NCT04344379
Recruitment Status :
(suspension of clinical trials with hydroxychloroquine by health authorities)
The Investigators propose to set up a preventive trial of infection in hospital workers at risk of coronavirus infection by comparing the rate of SARS-Cov-2 infection in a population of negative SARS-Cov-2 hospital workers receiving preventively azithromycin, hydroxychloroquine or a Placebo
Randomized clinical trial with 3 arms : hydroxychloroquine group, 300 subjects/azithromycin group, 300 subjects/ placebo of hydroxychloroquine group, 300 subjects. Hospital workers workers will be invited to participate in the study in each hospital and they will be included after giving their consent, assessment of their eligibility criteria, endonasal PCR and serolology at baseline. They will be randomized in one of the 3 arms, receive their treatment and will be followed by physical visit (at Day 2, Day 5, Day 15, Day 28) and by phone (at Day) 40 days with clinical data collection (tolerance and clinical signs of infection). At the end of treatment, another serology will be collected.
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Layout table for eligibility information
Ages Eligible for Study:
18 Years and older (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Hospital workers working at AP-HP hospitals over the age of 18
Hospital workers who have signed consent
No signs of COVID-19 infection
Women who are likely to procreate should have a negative pregnancy test on inclusion day. In addition, they should use at least one effective contraceptive method before starting treatment, during treatment and up to 8 months after the last drug tested during the trial. Sexually active men should also have effective contraception during treatment and for at least 8 months after the last drug tested during the trial.
Affiliated or beneficiary of Social Security
History of SARS-CoV-2 infection confirmed by PCR or serology is available at inclusion
A history of clinical episode suspecting a PCR-confirmed or unconfirmed COVID-19 infection.
Pregnancy and breastfeeding
Allergy or contraindications to one of the 2 drugs in the study
Long congenital QT syndrome (or known in the family)
QTc or 450 ms in men, or 460 ms in women, if Fc 55/mn (except in case of intense sport practice), if ESV on baseline ECG, if QRS - or 120 ms, if AC/FA, if the PR or BAV lengthening
History of severe ischemic heart disease or unbalanced heart failure.
Clinically significant bradycardia known
Known kidney or liver failure
Known G6PD deficit
Subject who received antiviral treatment in the 14 days prior to inclusion
Subject who had treatment with azithromycin or hydroxychloroquine, in the 14 days prior to inclusion
Hypokaliemia (<= 3.5 mmol/L), Increase in creatinine (>=120 micromol/Ll, Increase in transaminases at baseline (>=2N)