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HCQ for Primary Prophylaxis Against COVID19 in Health-care Workers

Primary Purpose

Sars-CoV2, Infection Viral, Healthcare Worker

Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Hydroxychloroquine
Placebo
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sars-CoV2

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Health-care worker with frequent contact with confirmed COVID-19 patients
  • No active or past infection with SARS-CoV-2
  • 18 years of age or older
  • No allergy or contraindication to hydroxychloroquine
  • written informed consent

Exclusion Criteria:

  • Age of less than 18 years
  • Pregnancy or lactation
  • unwillingness to use effective contraception during the participation in the trial
  • Use of concomitant medication that prolongs the QT interval
  • Allergy or contraindication to hydroxychloroquine
  • Retinopathy or maculopathy
  • Neuromuscular diseases (i.e Myasthenia gravis, Parkinson's disease)
  • G6PD Deficiency

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Hydroxychloroquine

    Placebo

    Arm Description

    200mg once daily

    Placebo

    Outcomes

    Primary Outcome Measures

    Symptomatic or asymptomatic SARS-CoV-2 infection confirmed by PCR

    Secondary Outcome Measures

    Viral load during SARS-CoV-2 infection
    Seroconversion during the study period
    Incidence of any acute respiratory infection
    Days of sick leave

    Full Information

    First Posted
    April 4, 2020
    Last Updated
    April 4, 2022
    Sponsor
    Medical University of Vienna
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04336748
    Brief Title
    HCQ for Primary Prophylaxis Against COVID19 in Health-care Workers
    Official Title
    Low-dose Hydroxychloroquine for Primary Prophylaxis Against SARS-CoV-2 in Health-care Workers - a Randomized, Double-blind, Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2022
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Not feasible
    Study Start Date
    April 2020 (Anticipated)
    Primary Completion Date
    July 2020 (Anticipated)
    Study Completion Date
    August 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Medical University of Vienna

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Background: Aim: To demonstrate the efficacy of low-dose hydroxychloroquine as primary prevention in healthcare workers Design, participants and interventions: Prospective, randomized, parallel group, double-blinded, placebo controlled, study. including 440 participants who will be randomised to 2 treatment arms: hydroxychloroquine or placebo. Outcome variables: symptomatic or asymptomatic SARS-CoV-2 infection confirmed by PCR, viral load during SARS-CoV-2 infection, seroconversion during the study period, incidence of any acute respiratory infection, days of sick leave. Statistical considerations: No trials have been published investigating the efficacy of HCQ as primary prophylaxis of SARS-CoV-2 infection in health care workers. Thus, sample size calculations in the proposed trial are based on the investigators' best estimates for several parameters. In accordance to the effect of oseltamivir against symptomatic influenza, we assumed an approximate effectiveness of approximately 60% (HR of 0.4) (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6464969/) as realistic. As a prophylactic intervention with HCQ, which may have side effects and for which supply shortage can be expected, was judged justifiable only if its effectiveness is high, we based our sample size consideration on a HR of 0.3. To estimate the probability of an event in both the experimental and the control group, very little data is available. In a Dutch point-prevalence study 0-10% of health-care workers were infected depending on the healthcare institution, depending on the hospital. This point-prevalence study was performed between 6 and 9 March, when the reported number of cases in the Netherlands was 33 and 77, respectively, according to the RIVM (https://www.rivm.nl/nieuws/resultaat-steekproef-4-ziekenhuismedewerkers-heeft-coronavirus). Additionally, in an a report published in the Lancet, 20% of responding healthcare workers in Italy were found to be infected with SARS-CoV2 within less than one month (https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)30627-9/fulltext). Several media reports indicate that this proportion is similar across various healthcare institutions and countries (https://www.nytimes.com/2020/03/24/world/europe/coronavirus-europe-covid-19.html) and (https://www.aljazeera.com/news/2020/03/spain-tightens-restrictions-week-lockdown-begins-200330191539568.html). As the proposed study will be performed in a high-risk setting, we assumed an event (i.e. PCR positivity) probability of 10% in the control group and 3% in the experimental arm after the maximum study period. In summary, a sample size of 210 participants per arm is necessary to detect a HR of 0.3 with a power of 80.3% with an alpha-error of 0.05. To account for drop-outs and asymptomatic, undetected infection at inclusion or past infection with existing immunity, an additional 10 participants will randomized per treatment arm. The overall study population is therefore 440 participants. Statistical analysis will be based on two populations: A Modified Intention to Treat population excluding those who withdrew consent after randomization and those with a positive serology at baseline. And a per protocol population including all randomized subjects who completed at least 3 out of 4 follow-up visits and took at least 80% of all doses of study medication.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Sars-CoV2, Infection Viral, Healthcare Worker, Prophylaxis

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Hydroxychloroquine
    Arm Type
    Active Comparator
    Arm Description
    200mg once daily
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo
    Intervention Type
    Drug
    Intervention Name(s)
    Hydroxychloroquine
    Intervention Description
    low dose (200mg) Hydroxychloroquine once daily for 4 weeks
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    Placebo
    Primary Outcome Measure Information:
    Title
    Symptomatic or asymptomatic SARS-CoV-2 infection confirmed by PCR
    Time Frame
    4 weeks
    Secondary Outcome Measure Information:
    Title
    Viral load during SARS-CoV-2 infection
    Time Frame
    4 weeks
    Title
    Seroconversion during the study period
    Time Frame
    4 weeks
    Title
    Incidence of any acute respiratory infection
    Time Frame
    4 weeks
    Title
    Days of sick leave
    Time Frame
    4 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Health-care worker with frequent contact with confirmed COVID-19 patients No active or past infection with SARS-CoV-2 18 years of age or older No allergy or contraindication to hydroxychloroquine written informed consent Exclusion Criteria: Age of less than 18 years Pregnancy or lactation unwillingness to use effective contraception during the participation in the trial Use of concomitant medication that prolongs the QT interval Allergy or contraindication to hydroxychloroquine Retinopathy or maculopathy Neuromuscular diseases (i.e Myasthenia gravis, Parkinson's disease) G6PD Deficiency

    12. IPD Sharing Statement

    Learn more about this trial

    HCQ for Primary Prophylaxis Against COVID19 in Health-care Workers

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