Skip to main content
OpenTrials
Completed

NCT Number: NCT04334148

Healthcare Worker Exposure Response and Outcomes of Hydroxychloroquine

This is a double blind, placebo controlled study in approximately 2,000 health care workers at risk for being exposed to COVID-19. Eligible participants will be randomly assigned (1:1) to either treatment group (HCQ) or placebo in a double-blind fashion. Course of treatment is 30 days.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Children's Hospital Colorado/University of Colorado Denver, Aurora, Colorado, United States

Loading trial locations.

About this study

This is a double blind, placebo controlled study in approximately 2,000 health care workers at risk for being exposed to COVID-19. Eligible participants will be randomly assigned (1:1) to either treatment group (HCQ) or placebo in a double-blind fashion. After enrollment, baseline assessments will include nasopharyngeal swab for COVID-19 and a blood sample to detect seroconversion to COVID-19. For convenience, follow-up will be performed weekly through a direct to participant portal. A call center will provide support for any missed visits. Follow-up includes screening for any COVID-19 clinical infections, other respiratory infections, clinical events, adverse events, and Quality of Life (QoL) assessments. Course of treatment is 30 days. Participants are followed via survey weekly. At the end of treatment participants will return for repeat nasopharyngeal swab for COVID-19 and a blood sample to detect seroconversion to COVID-19. There will be one last contact at 8 weeks (2 months) from baseline.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion:

  • Completed Informed Consent
  • Age ≥ 18 years old
  • Currently working in any environment in which there is a risk of exposure to patients with COVID-19 infections ("healthcare worker")

Exclusion criteria

  • Prior diagnosis of COVID-19 infection
  • Participation in another COVID-19 prophylaxis trial within 30 days of consent
  • Respiratory illness with new-onset fever (Temperature > 100°F) or ongoing cough or dyspnea within 14 days
  • Known allergy to HCQ or chloroquine
  • Congenital prolonged QT syndrome
  • Current or planned use of QT prolonging drugs (e.g. procainamide, disopyramide, mexiletine, flecainide, propafenone, amiodarone, sotalol, cimetidine, dronedarone, dofetilide, levofloxacin, ciprofloxacin, moxifloxacin) and other contraindicated medications
  • End stage renal disease
  • Pre-existing retinopathy
  • Current or planned use of Hydroxychloroquine (study drug) for any indication

Current or planned use of the following for treatment or prevention of COVID-19 infection:

  • Chloroquine
  • Azithromycin
  • Known cirrhosis or severe liver disease
  • History of severe skin reactions such as Steven-Johnson syndrome, toxic epidermal necrolysis
  • History of psoriasis or porphyria
  • Ventricular arrhythmias requiring medical treatment
  • Severe coronary artery disease or heart failure/cardiomyopathy with ongoing symptoms
  • Current or planned use of use of anti-seizure drugs
  • History of Glucose-6-phosphate dehydrogenase deficiency

Treatment and study plan

Hydroxychloroquine

Drug

oral self administered tablet

Other names: Plaquenil

Placebo oral tablet

Drug

oral self administered tablet

Primary outcomes

  1. Number of Participants With Clinical Infection With COVID-19 Infection

    Time frame: 30 days

    This measure was a combination of confirmed infection and suspected infection. Confirmed clinical infection was defined as new-onset of fever or cough or dyspnea AND confirmed COVID-19 positive test result via local PCRI testing. Suspected infection was defined as new-onset fever or cough or dyspnea without local PCR testing due to local restrictions and/or testing policies.

Secondary outcomes

  1. Number of Participants With COVID-19 Viral Shedding

    Time frame: 30 days

    Number of participants with COVID-19 infection shedding via Covance swab PCR testing

  2. Number of Participants With Serious Adverse Events (SAEs) or Hydroxychloroquine-Associated Events of Special Interest (EOSIs)

    Time frame: 30 days

    Safety and Tolerability as determined by subject reported serious adverse events (SAEs) and hydroxychloroquine-associated events of special interest. EOSIs include: arrhythmias (ventricular), hepatic failure, bone marrow failure, aplastic anemia, prolonged QT interval, angioedema, dermatitis exfoliative, acute generalized exanthematous pustulosis, psychosis, suicidal ideation, seizure, methemoglobinemia.

Sponsors and collaborators

Lead sponsor

Adrian Hernandez

Other

Collaborators

  • Patient-Centered Outcomes Research Institute

Registry information

Official study title

Healthcare Worker Exposure Response and Outcomes of Hydroxychloroquine Trial (HERO-HCQ Trial)

Acronym: HERO-HCQ

Important dates

Study start
2020
Primary completion
2020
Study completion
2021
First posted
Apr 6, 2020
Registry last updated
Oct 12, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.