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Melatonin for Treatment of Delirium in Critically Ill Adult Patients

Delirium

The purpose of this study is to determine the feasibility of conducting a randomized controlled trial (RCT) with melatonin for treatment of delirium in critically ill adult patients. From a feasibility perspective, the investigators believe that the proposed design will achieve the minimum enrollment rate necessary to conduct a future RCT on a larger scale.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Patients aged 18 years or older admitted to the intensive care unit;
* Anticipated ICU stay \> 48 hours;
* ICDSC score greater than or equal to 4 for a maximum of 48 hours prior to randomization.

Exclusion Criteria:

* Known allergy or hypersensitivity to melatonin or to ingredients in ORA-BLEND SF®;
* Use of melatonin within 24 hours prior to randomization;
* Presence of severe structural brain injury (intracranial hemorrhage or traumatic brain injury), severe major neurocognitive disorder, advanced neurodegenerative disease or hepatic encephalopathy;
* Diagnosis of schizophrenia, bipolar affective disorder, psychotic depression, uremic encephalopathy or alcohol withdrawal;
* Presence of active seizures, coma, aphasia or severe intellectual disability;
* Limited short-term vital prognosis;
* Diagnosis of delirium prior to ICU admission;
* Pregnancy or breastfeeding;
* Absolute contraindication to receive enteral medication;
* Inability to understand or speak English or French;
* Total blindness.

Study Location

Hopital Maisonneuve-Rosemont
Hopital Maisonneuve-Rosemont
Montréal, Quebec
Canada

Contact Study Team

Backup Contact

Marianne Leblanc, Pharm.D.

Backup Contact

Winnie Tran, Pharm.D.

Backup Contact

Katerine Chalifoux, Pharm.D.

Backup Contact

Aryane Roy, B.Pharm.

Backup Contact

Mounia Louerguioui, Pharm.D.

Primary Contact

Johannie Beaucage-Charron, Pharm.D., M.Sc.

Backup Contact

Patricia Poirier, Pharm.D.

Study Sponsored By
Ciusss de L'Est de l'Île de Montréal
Participants Required
More Information
Study ID: NCT05713877