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Completed

NCT Number: NCT04328480

The ECLA PHRI COLCOVID Trial. Effects of Colchicine on Moderate/High-risk Hospitalized COVID-19 Patients.

The ECLA PHRI COLCOVID Trial is a simple, pragmatic randomized open controlled trial to test the effects of colchicine on moderate/high-risk hospitalized COVID-19 patients with the aim of reducing mortality and/or new requirement for mechanical ventilation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Sanatorio Parque

Rosario, Santa Fe Province, 2000, Argentina

About this study

Various anti-viral treatments are being tested in clinical trials worldwide. The World Health Organization (WHO) launched a simple,pragmatic worldwide open-label trial to test Remdesivir, Lopinavir/Ritonavir, Interferon and Hydroxychloroquine or Chloroquine.The most important complication of COVID-19 severe cases is respiratory failure from severe acute respiratory syndrome (SARS), the leading cause of mortality. Accumulating evidence suggests that patients with severe COVID-19 might have a cytokine storm syndrome, a hyperinflammatory syndrome characterized by a fulminant and fatal hypercytokinemia and multiorgan failure.

The proposed pathophysiological mechanism of cytokine storm and inflammatory cascade activation is based on evidence collected primarily during the SARS-CoV and MERS-CoV epidemics (with a significant increase in IL1B, IL6, IL12, IFNγ, IP10, TNFα, IL15, and IL17 among others). The data collected during the pandemic with COVID-19 also shows a significant increase in inflammatory cytokines (GCSF, IP10, MCP1, MIP1A, and TNFα, among others) in sicker patients admitted to intensive care. In the absence of effective treatments for the management of patients with COVID-19 and respiratory failure, the immunomodulatory and anti-inflammatory effect of colchicine on cytokines involved in the hyper-inflammatory state is postulated. Several lines of research worldwide are testing powerful anti-inflammatory drugs for the pandemic, with different options including steroids, cytokine blockers, and other potent anti-inflammatory agents. Steroids are partially contraindicated in viral infections.

Colchicine is a powerful anti-inflammatory drug approved for the treatment or prevention of gout and Familial Mediterranean Fever at doses ranging between 0.3 mg and 2.4 mg/day. Its mechanism of action is through the inhibition of tubulin polymerization, as well as through potential effects on cellular adhesion molecules and inflammatory chemokines. It might also have direct anti-inflammatory effects by inhibiting key inflammatory signalling networks known as inflammasome and pro-inflammatory cytokines. Additionally, evidence suggests that colchicine exerts a direct anti-inflammatory effect by inhibiting the synthesis of tumor necrosis factor alpha and IL-6, monocyte migration, and the secretion of matrix metalloproteinase-9. Through the disruption of the cytoskeleton, colchicine is believed to suppress secretion of cytokines and chemokines as well as in vitro platelet aggregation. All these are potentially beneficial effects that might diminish or ameliorate the COVID-19 inflammatory storm associated with severe forms of the disease. Importantly, in one contemporary trial low-dose colchicine administered to patients who survived from acute coronary syndrome shows a statistically significantly reduction of cardiovascular complications.

We have therefore designed in a simple, pragmatic randomized controlled trial to test the effects of colchicine on severe hospitalized COVID-19 cases with the aim of reducing mortality.

Sample size calculation:

A minimum sample size of 1200 patients will provide 80% power to detect a relative risk reduction of approximately 30% in the treated group if the assumed composite rate (new requirement of intubation and / or death) in the control group is about 24%.

The ECLA PHRI COLCOVID Trial allows randomization to another trial, specifically patients included in the trial might be (or not) randomized to an antithrombotic strategy.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

(case definition)

  • Consented adults (age ≥18 years) and
  • COVID-19 suspicious and
  • Admitted to hospital or already in hospital and
  • COVID-19 suggestive symptoms (fever or febrile equivalent, loss of smell and taste, fatigue, etc.) that may be present or absent at randomization time and
  • SARS (severe acute respiratory syndrome)
  • shortness of breath (dyspnea) or
  • image of typical or atypical pneumonia or
  • oxygen desaturation (SpO2 ≤ 93)

Exclusion criteria

  • Clear indication or contraindication for the use of colchicine
  • Pregnant or breastfeeding female.
  • Chronic renal disease with creatinine clearance <15 ml/min/m2
  • Negative PCR test for SARS-COV2

Treatment and study plan

Colchicine

Drug

The colchicine dosage schedule will vary according to the following scenarios:

  • In patients not receiving Lopinavir/Ritonavir
  • Loading dose of 1.5 mg followed by 0.5 mg after two hours (day 1)
  • The next day 0.5 mg bid for 14 days or until discharge.
  • In patients receiving Lopinavir/Ritonavir
  • Loading dose of 0.5 mg (day 1)
  • After 72 hours from the loading dose, 0.5 mg every 72 hours for 14 days or until discharge.
  • Patients under treatment with Colchicine that are starting with Lopinavir/Ritonavir
  • Dose of 0.5 mg 72 hours after starting Lopinavir/Ritonavir.
  • Continue with 0.5 mg every 72 hours for 14 days or until discharge.

Only the oral route will be used except in the case of patients associated with mechanical ventilation or with contraindications to the oral route, in whom it will be administered by nasogastric tube.

Other names: Colchicina

Local standard of care

Other

Local standard of care for COVID-19 SARS moderate /high-risk patients

Primary outcomes

  1. Composite outcome: New requirement for mechanical ventilation or death

    Time frame: 28 days post randomization

    Number of participants who require new intubation for mechanical ventilation or die

  2. Mortality

    Time frame: 28 days post randomization

    Number of participants who die

Secondary outcomes

  1. New requirement for mechanical ventilation or death from respiratory failure

    Time frame: 28 days post randomization

    Number of participants who require new intubation for mechanical ventilation or die from respiratory failure

  2. New requirement for mechanical ventilation or death from non-respiratory failure

    Time frame: 28 days post randomization

    Number of participants who require new intubation for mechanical ventilation or die from non-respiratory failure

  3. Mortality due to respiratory failure

    Time frame: 28 days post randomization

    Number of participants who die from respiratory failure

  4. Mortality due to non-respiratory failure

    Time frame: 28 days post randomization

    Number of participants who die from non-respiratory failure

  5. In hospital - Composite outcome

    Time frame: During hospitalization or until death, whichever comes first, assessed up to 28 days

    Number of participants who require intubation for mechanical ventilation or die

  6. In hospital - Mortality

    Time frame: During hospitalization or until death, whichever comes first, assessed up to 28 days

    Number of participants who die

  7. Composite outcome (New requirement for mechanical ventilation or death) evaluated in Non-intubated population

    Time frame: 28 days post randomization

    Number of participants who were not intubated at randomization and require new intubation for mechanical ventilation or die

  8. Mortality evaluated in Non-intubated population

    Time frame: 28 days post randomization

    Number of participants who were not intubated at randomization and die

  9. Mean WHO descriptive score of COVID-19 during hospitalization

    Time frame: During hospitalization or until death, whichever comes first, assessed up to 28 days

    Mean WHO descriptive score of COVID-19 in the active treatment group compared to the placebo group

  10. Highest WHO descriptive score of COVID-19 during hospitalization

    Time frame: During hospitalization or until death, whichever comes first, assessed up to 28 days

    Mean highest WHO descriptive score of COVID-19 in the active treatment group compared to the placebo group

Sponsors and collaborators

Lead sponsor

Estudios Clínicos Latino América

Other

Collaborators

  • Population Health Research Institute

Registry information

Official study title

The ECLA PHRI COLCOVID Trial

Acronym: COLCOVID

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Mar 31, 2020
Registry last updated
Apr 27, 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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