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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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04751227
Enrollment
8
Registered
2021-02-12
Start date
2020-11-22
Completion date
2021-01-30
Last updated
2021-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Dysfunction, COVID-19, Critical Illness

Brief 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.

Interventions

DRUGModafinil

100-200 mg oral daily for for Wakefulness in the Critical Care Units

Sponsors

King Faisal Specialist Hospital & Research Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years

Inclusion criteria

1. ICU patients 18 years and older 2. admitted to COVID and non-COVID units between January 2017 and June 2020 3. ICU stay for at least 48 hours 4. started on modafinil during ICU stay for at least 48 h 5. required ventilatory support.

Exclusion criteria

* Those who did not receive modafinil or received modafinil for indications other than ICU wakefulness

Design outcomes

Primary

MeasureTime frameDescription
Median change in of Glasgow Coma Scale (GCS)48 hours before modafinil therapy and 7 days after modafinil therapyDescribe the median change in Glasgow Coma Scale (GCS) before and after modafinil therapy. The GCS is used to assess and communicate changes in mental status and to measure the duration of coma. The Glasgow Coma Scale is comprised of the individual components, e.g. eye(4) verbal(5) motor (6). Glasgow Coma Score is calculated by addition of the total points selected under each component (eye, verbal, motor) score can range from 1 and 15

Secondary

MeasureTime frameDescription
adverse drug reactions (ADRs)until ICU discharge, 90 days or death whichever occurs first.Number of patients started on antipsychotics and with possible adverse drug reactions (ADRs) related to modafinil including nervousness, agitation, delirium, hypersensitivity, and drug rash. Naranjo scale was used to evaluate the causality of ADRs and modafinil therapy
Duration of Mechanical VentilationFrom Intubation to extubation date and off Mechanical Ventilation or until ICU discharge, death, or 90 days whichever occurs first. ]To assess whether modafinil can help to shorten the time of being in breathing tube and ventilator (duration of mechanical ventilation )
ICU Length of stay (LOS)until ICU discharge, 90 days or death whichever occurs first.To describe ICU LOS
Hospital Length of Stay (LOS)until hospital discharge, 90 days or death whichever occurs first.To describe hospital LOS
Mortality rate28 days and 90 daysDeath that occurs during 28 days and 90 days

Countries

Saudi Arabia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026