Skip to main content
OpenTrials
Completed

NCT Number: NCT04568863

Efficacy of Intravenous Melatonin on Mortality in Adult Patients Admitted to the Intensive Care Unit With COVID-19

There is an urgent need to evaluate effective treatments for COVID-19 patients. Melatonin has significant anti-inflammatory and antioxidant properties and it lacks of side-effects. This randomized controlled trial seeks to evaluate the efficacy of intravenous melatonin in reducing mortality in Covid-19 patients in the ICUs.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hospital Universitario La Paz

Madrid, 28046, Spain

About this study

ICU COVID-19 patients show high risk of death mainly due to sepsis and respiratory disfunction. Prevention of these critical conditions is mandatory to reduce mortality and to improve patient's outcome.

Melatonin is an endogenous hormone involved not only in circadian rhythm control, but also in the cell protection due to its outstanding anti-inflammatory and antioxidative effects. High doses of melatonin have shown high efficacy against bacterial (sepsis) and viral infections. Melatonin is a safe product that consistently has shown lack of side-effects when it is administered to humans.

SARS-CoV 2 infection may yield severe forms of the disease that require the patients admission to the ICU. These patients may develop an excessive inflammatory response and a burst of free radicals, constituting the major cause of death in these subjects.

Our hypothesis is that high doses of melatonin intravenously administered to COVID-19 ICU patients might reach enough blood levels able to prevent/counteract the developing of sepsis and the production of free radicals, reducing mortality and hospital stay.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patient, family member or legal guardian has provided written Informed Consent.
  • Age ε 18 years.
  • Confirmed SARS-CoV-2 infection with compatible symptoms AND a positive RT-PCR.
  • Admission to the ICU with acute hypoxemic respiratory failure attributed to SARS-CoV-2 infection.
  • ICU length of stay of less than 7 days prior to randomization with or without MV and without signs of improvement in respiratory failure (MURRAY score at randomization greater or equal to the MURRAY score at ICU admission).

Exclusion criteria

  • Participant in a different COVID-19 study in which the study drug is under clinical development and hasn't been previously authorized for commercialization.
  • Liver enzymes > 5 times the upper normal range.
  • Chronic kidney disease with GFR < 30 mL/min/1.73 m2 (stage 4 or greater) or need for hemodialysis.
  • Pregnancy. A pregnancy test will be performed on every woman younger than 55 years of age prior to inclusion.
  • Terminal surgical or medical illness.
  • Autoimmune disease.
  • Any patient condition that can prevent the study procedures to be carried out at the treating physician's judgement.

Treatment and study plan

Melatonin intravenous

Drug

7 days of 5 mg per Kg of actual body weight per day of intravenous melatonin every 6 hours. Maximum daily dose 500 mg per day.

Placebo Intravenous

Drug

7 days of 5 mg per Kg of actual body weight per day of intravenous identically-looking placebo every 6 hours.

Primary outcomes

  1. Mortality

    Time frame: one month

    Mortality in each study group represented in frequency and time-to-event at day 28 after randomization

Sponsors and collaborators

Lead sponsor

Pharmamel S.L.

Industry

Collaborators

  • Hospital Universitario La Paz
  • Instituto de Investigación Hospital Universitario La Paz

Registry information

Official study title

A Phase II, Single-center, Double-blind, Randomized Placebo-controlled Trial to Explore the Efficacy and Safety of Intravenous Melatonin in Patients With COVID-19 Admitted to the Intensive Care Unit (MelCOVID Study)

Acronym: MELCOVID

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Sep 29, 2020
Registry last updated
Mar 18, 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.