Official Title
Amiodarone or Verapamil in COVID-19 Hospitalized Patients With Symptoms
Brief Summary

There is an urgent need for effective therapies against the novel COVID-19 virus. Studies have shown that amiodarone and verapamil can interfere with coronavirus entry and amplification by blocking ion channels. ReCOVery-SIRIO is a randomized study to investigate amiodarone or verapamil compared with usual care in symptomatic patients hospitalized with confirmed COVID-19 infection.

Completed
COVID-19

Drug: Amiodarone

Ion channel blocker

Drug: Verapamil

Ion channel blocker

Eligibility Criteria

Inclusion Criteria:

Hospitalized patients with confirmed COVID-19 infection and symptoms, with an oxygenation
index defined as quotient of partial pressure of oxygen in arterial blood (PaO2, in mmHg)
and fraction of inspired oxygen (FiO2) > 200.

Exclusion Criteria:

- Acute respiratory distress syndrome (ARDS)

- Contraindications for or known hypersensitivity to amiodarone or calcium channel
blockers

- Long QT syndrome

- Prolonged baseline QTc interval (≥450 ms).

- Cardiogenic shock or severe hypotension (SBP< 90 mmHg)

- Severe left ventricle dysfunction (left ventricular ejection fraction ≤35%)

- Severe sinus - node dysfunction with marked sinus bradycardia

- 2nd/3rd degree heart block

- Bradycardia without pacemaker that has caused syncope

- History of severe dysthyroidism

- A-Fib/flutter conducted via accessory pathway (ie,Wolff -Parkinson-White)

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 99 Years
Countries
Poland
Locations

Nicolaus Copernicus University
Bydgoszcz, Poland

Nicolaus Copernicus University
NCT Number
MeSH Terms
COVID-19
Amiodarone
Verapamil