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Withdrawn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

About this trial
This is an interventional prevention trial for Sars-CoV2
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
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
NCT ID
NCT04336748
First Posted
April 4, 2020
Last Updated
April 4, 2022
Sponsor
Medical University of Vienna
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Withdrawn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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