Clinical Trials Directory

Trials / Completed

CompletedNCT04751227

Modafinil for Wakefulness in the Critical Care Units

Modafinil for Wakefulness in the Critical Care Units and COVID-19 Patients at a Tertiary Care Saudi Hospital

Status
Completed
Phase
Study type
Observational
Enrollment
8 (actual)
Sponsor
King Faisal Specialist Hospital & Research Center · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers

Summary

It has been well documented that patients in the intensive care unit (ICU) are susceptible to developing neurocognitive and musculoskeletal complications because of various factors, including the nature of the critical illness, medications, over-sedation, and pain. Neuro-stimulants are used to speed up physical and mental processes through the increase in neurotransmitter, which translates into increase in arousal, wakefulness, attention, memory, mental and motor processing speed. The investigators reviewed the literature and described the clinical characteristics for a case series of adult patients admitted to COVID and non-COVID ICU between January 2017 and June 2020, who received modafinil to promote wakefulness and improve cognition at the King Faisal Specialist Hospital and Research Centre (KFSH\&RC) in Riyadh, Saudi Arabia. The secondary goals to describe the change of Glasgow Coma Scale (GCS) before and after the start of modafinil therapy, ICU and hospital length of stay, discharge disposition, adverse drug effects, and mortality rate.

Conditions

Interventions

TypeNameDescription
DRUGModafinil100-200 mg oral daily for for Wakefulness in the Critical Care Units

Timeline

Start date
2020-11-22
Primary completion
2021-01-30
Completion
2021-01-30
First posted
2021-02-12
Last updated
2021-02-12

Locations

1 site across 1 country: Saudi Arabia

Regulatory

Source: ClinicalTrials.gov record NCT04751227. Inclusion in this directory is not an endorsement.