Evidence map›Paper›PMID 38715471›Full record

Trial reportNeuropsychopharmacology reports2024

Evaluation of the effect of Modafinil in the improvement of the level of consciousness in patients with COVID-19 encephalopathy: A randomized controlled trial.

Fatemeh Talebi Kiasari, Mobin Naghshbandi, Maziar Emamikhah, Omid Moradi Moghaddam, Mohammad Niakan Lahiji, Mohammad Rohani, Narges Yazdi, Hamidreza Movahedi, Alireza Amanollahi, Pardis Irandoost and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Fatemeh Talebi KiasariDepartment of Neurology, Hazrat-e Rasool General Hospital, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mobin NaghshbandiSchool of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Maziar EmamikhahDepartment of Neurology, Hazrat-e Rasool General Hospital, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Omid Moradi MoghaddamTrauma and Injury Research Center, Critical Care Department, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mohammad Niakan LahijiTrauma and Injury Research Center, Critical Care Department, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mohammad RohaniDepartment of Neurology, Hazrat-e Rasool General Hospital, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Narges YazdiDepartment of Neurology, Hazrat-e Rasool General Hospital, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Hamidreza MovahediSchool of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Alireza AmanollahiTrauma and Injury Research Center, Critical Care Department, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Pardis IrandoostDepartment of Nutrition, School of Public Health, Iran University of Medical Sciences, Tehran, Iran.
Roya GhafourySchool of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-1825-1284

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimCOVID-19 can lead to encephalopathy and loss of consciousness. This double-blinded randomized clinical trial conducted in Tehran, Iran, aimed to assess the potential effectiveness of modafinil in patients with COVID-19-related encephalopathy.

methodsNineteen non-intubated COVID-19 patients with encephalopathy were randomized into two groups: a treatment group receiving crushed modafinil tablets and a placebo group receiving starch powder. Modafinil was administered at a dose of 100 mg every 2 h, reaching a peak dosage of 400 mg. The level of consciousness was assessed using the Glasgow Coma Score (GCS) at multiple time points on the day of medication administration. The trial was registered under IRCT20170903036041N3 on 23/5/2021.

resultsThe average age in the modafinil and placebo groups was 75.33 and 70 years, respectively. No significant differences were observed between the two groups in terms of chronic conditions, clinical symptoms, or laboratory data. GCS scores were similar between the groups at baseline (p-value = 0.699). After four doses of modafinil, GCS scores were slightly higher in the treatment group, but this difference was not statistically significant (p-value = 0.581). GCS scores after each round of drug administration didn't significantly differ between the treatment and placebo groups (p-value = 0.908).

conclusionModafinil exhibited a slight improvement in the level of consciousness among COVID-19 patients with encephalopathy, although this improvement did not reach statistical significance when compared to the control group. Further research with larger sample sizes and longer treatment durations is recommended to explore modafinil's potential benefits in managing altered consciousness in COVID-19 patients.

Indexed as

ConsciousnessCOVID-19ModafinilAgedAged, 80 and overBrain DiseasesCOVID-19 Drug TreatmentDouble-Blind MethodFemaleGlasgow Coma ScaleHumansIranMaleMiddle AgedSARS-CoV-2Treatment OutcomeModafinilWakefulness-Promoting AgentsCOVID‐19encephalopathyloss of consciousnessModafinil

Identifiers

PMID38715471
PMCPMC11544445

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.