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Completed

NCT Number: NCT04321278

Safety and Efficacy of Hydroxychloroquine Associated With Azithromycin in SARS-CoV2 Virus (Coalition Covid-19 Brasil II)

The Severe Acute Respiratory Syndrome COronaVirus 2 (SARS-CoV2) is a new and recognized infectious disease of the respiratory tract. Around 20% of those infected have severe pneumonia and currently there is no specific or effective therapy to treat this disease. Therapeutic options using malaria drugs chloroquine and hydroxychloroquine have shown promising results in vitro and in vivo test. But those efforts have not involved large, carefully-conducted controlled studies that would provide the global medical community the proof that these drugs work on a significant scale. In this way, the present study will evaluate the effectiveness and safety of the use of hydroxychloroquine combined with azithromycin compared to hydroxychloroquine monotherapy in patients hospitalized with pneumonia by SARS-CoV2 virus.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Hospital de Urgência e Emergência de Rio Branco, Rio Branco, Acre, Brazil

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About this study

The Severe Acute Respiratory Syndrome COronaVirus 2 (SARS-CoV2) is a new and recognized infectious disease of the respiratory tract that is now spreading to several countries in the world, including Brazil. Mortality rates after infection are higher in adults over 60 and with a history of comorbidities. The most serious patients need care in intensive care units (ICU). Most of the time they depend on mechanical ventilation support due to acute respiratory distress syndrome (ARDS). Infection rates are higher than the capacity for intensive care, which represents a serious problem in medical care. Around 20% of those infected have severe pneumonia and so far it does not have a specific therapy, or even, an effective clinical management. Therapeutic options using malaria drugs chloroquine and hydroxychloroquine have shown promising results in vitro and in vivo test. A recent, small, non-randomized study with hydroxychloroquine in 36 patients infected with SARS-Cov-2 proved to be promising in the ability to reset the viral load in 6 days after starting treatment. Thus, the present study will evaluate the effectiveness and safety of the use of hydroxychloroquine combined with azithromycin compared to hydroxychloroquine monotherapy in the clinical evolution by the ordinal scale of 6 points in adult patients hospitalized with pneumonia caused by infection by the SARS-CoV2 virus in Brazil.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Males and females aged > 18 years;
  • Suspected or confirmed infection by SARS-CoV2;

Presenting with one of the following:

  • Need for oxygen supplementation > 4 L/min, or
  • Need for high-flow nasal canula, or
  • Need for non-invasive ventilation, or
  • Need for mechanical ventilation.

Exclusion criteria

  • Refusal to provide written informed consent (either the patient or a legal representative);
  • Hypersensitivity to any of the drugs used in the study (Azithromycin or Hydroxychloroquine);
  • Patients with more than 48 hours of prior study medication use;
  • Patients with onset of symptoms longer than 14 days;
  • Patients with long QT syndrome or severe ventricular arrhythmias, not protected by an implantable cardioverter defibrillators (ICD).;
  • QTc>= 480ms;
  • Do not resuscitate order or exclusive palliative care;
  • Patients with liver disease or cirrhosis or abnormal liver enzyme tests above three times the upper limit values (alanine aminotransferase -ALT and aspartate aminotransferase - AST);
  • Patients with known retinopathy or macular degeneration;
  • Patients with history of pancreatitis;
  • Patients with concomitant use of medications that alter the absorption or excretion of azithromycin or hydroxychloroquine;
  • Breastfeeding women;
  • Pregnancy

Treatment and study plan

Hydroxychloroquine + azithromycin

Drug

Intervention Group: Hydroxychloroquine + azithromycin. After randomization, Hydroxychloroquine [400mg 2x/day, 12/12h] + azithromycin [500mg 1x/day]) for 10 days. Standard treatment is according to the treatment protocol for 2019-nCoV infection.

Other names: HCQ+AZI

Hydroxychloroquine

Drug

Active Control Group: Hydroxychloroquine. After randomization, Hydroxychloroquine [400mg 2x/day, 12/12h] for 10 days. Standard treatment is according to the treatment protocol for 2019-nCoV infection.

Other names: HCQ

Primary outcomes

  1. Evaluation of the clinical status

    Time frame: 15 days after randomization

    Evaluation of the clinical status of patients on the 15th day after randomization defined by the Ordinal Scale of 6 points (score ranges from 1 to 6, with 6 being the worst score)

Secondary outcomes

  1. All-cause mortality

    Time frame: 29 days after randomization

    All-cause mortality rates at 29 days after randomization

  2. Evaluation of the clinical status

    Time frame: 7 and 29 days after randomization

    Evaluation of the clinical status of patients on the 7th and 29th day after randomization defined by the Ordinal Scale of 6 points (score ranges from 1 to 6, with 6 being the worst score)

  3. Number of days free from mechanical ventilation

    Time frame: 29 days after randomization

    Number of days free from mechanical ventilation at 29 days after randomization

  4. Duration of mechanical ventilation

    Time frame: 29 days after randomization

    Number of days that the patient was on mechanical ventilation after randomization

  5. Duration of hospitalization

    Time frame: 29 days after randomization

    Length of hospital stay on survivors

  6. Other secondary infections

    Time frame: 29 days after randomization

    Presence of other secondary infections

  7. Time from treatment start to death

    Time frame: 29 days after randomization

    Time from treatment start to death

  8. Medium and long-term outcomes of SARS-CoV2 infection on morbimortality, daily life activities, mental health, and quality of life

    Time frame: 3, 6, 9 and 12 months

    Morbimortality, daily life activities, mental health, and quality of life

  9. Assess whether the tested therapies may be affected by leucocyte phenotype

    Time frame: Baseline

    Leucocyte transcriptome

Other outcomes

  1. QT interval prolongation

    Time frame: 29 days after randomization

    Occurrence of QT interval prolongation

  2. Gastrointestinal intolerance

    Time frame: 29 days after randomization

    Occurrence of gastrointestinal intolerance

  3. Laboratory abnormalities

    Time frame: 29 days after randomization

    Occurrence of laboratory hematimetric parameters, creatinine and bilirubin

  4. Adverse events

    Time frame: 29 days after randomization

    Occurrence of adverse events related to the use of the investigational products

Sponsors and collaborators

Lead sponsor

Hospital Israelita Albert Einstein

Other

Collaborators

  • Brazilian Research In Intensive Care Network
  • EMS
  • Hospital Sirio-Libanes
  • Hospital do Coracao

Registry information

Official study title

Evaluation of the Safety and Clinical Efficacy of Hydroxychloroquine Associated With Azithromycin in Patients With Pneumonia Caused by Infection by the SARS-CoV2 Virus - Coalition COVID-19 Brasil II - SEVERE - Patients

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Mar 25, 2020
Registry last updated
Jan 20, 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.

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