Evidence map›Paper›PMID 40205270›Full record

Trial reportInflammopharmacology2025

Repurposing of high-dose N-acetylcysteine as anti-inflammatory, antioxidant and neuroprotective  agent  in moderate to severe traumatic brain injury patients: a randomized controlled trial.

Alaa Refaat Gouda, Noha A El-Bassiouny, Ahmad Salahuddin, Emad Hamdy Hamouda, Amira B Kassem

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Inflammopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
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

5 authors.

Alaa Refaat GoudaClinical Pharmacy and Pharmacy Practice Department, Faculty of Pharmacy, Damanhour University, Damanhour, 22514, Egypt. a.youssef00925@pharm.dmu.edu.eg.ORCID http://orcid.org/0009-0009-7331-4848
Noha A El-BassiounyClinical Pharmacy and Pharmacy Practice Department, Faculty of Pharmacy, Damanhour University, Damanhour, 22514, Egypt.ORCID http://orcid.org/0000-0001-9277-2910
Ahmad SalahuddinBiochemistry Department, Faculty of Pharmacy, Damanhour University, Damanhour, 22514, Egypt.ORCID http://orcid.org/0000-0002-7382-4284
Emad Hamdy HamoudaCritical Care Medicine Department, Faculty of Medicine, University of Alexandria, Alexandria, 21517, Egypt.ORCID http://orcid.org/0009-0009-9864-9230
Amira B KassemClinical Pharmacy and Pharmacy Practice Department, Faculty of Pharmacy, Damanhour University, Damanhour, 22514, Egypt. Amira.kassem@pharm.dmu.edu.eg.ORCID http://orcid.org/0000-0003-4195-6036

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTraumatic brain injury (TBI) refers to an impact of the brain within the skull resulting in an altered mental state. The study aim is to determine the effect of a high dose of N-acetylcysteine (NAC) on biochemical and inflammatory markers of neuronal damage and clinical outcomes in patients with moderate to severe TBI.

methodsA randomized open label-controlled trial was conducted on 40 patients with moderate to severe TBI patients presented to the emergency unit within < 24 h since the trauma occurred and randomized into NAC and control groups 20 patients each. Serum samples for evaluation of biomarkers: malondialdehyde (MDA), interleukin-6 (IL-6), neuron-specific enolase (NSE), and S100B were withdrawn at baseline and on day 7. The patients were followed for 7 days and evaluated clinically by the Glasgow Coma Scale (GCS).

resultsThere was a significant decrease in NSE and MDA levels on day 7 from baseline in NAC group (p < 0.001 and p < 0.001). Also, S100B and IL-6 decreased significantly in NAC group on day 7 from baseline (p = 0.003 and p < 0.001 consequently) compared to control group. Moreover, patients in NAC group showed a significantly shorter length of stay at intensive care unit (ICU) (p = 0.038). There was a significant increase in GCS in NAC group on day 7 from baseline (p = 0.001).

conclusionAdjunctive early use of high-dose NAC significantly reduced inflammatory and oxidative markers and had neuroprotective effect which may be a novel treatment option for moderate to severe TBI patients.

trial registrationPactr.org identifier: (PACTR202209548995270) on 14 September 2022.

Indexed as

AcetylcysteineAnti-Inflammatory AgentsAntioxidantsBrain Injuries, TraumaticNeuroprotective AgentsAdultBiomarkersDrug RepositioningFemaleGlasgow Coma ScaleHumansInterleukin-6MaleMalondialdehydeMiddle AgedPhosphopyruvate HydrataseAcetylcysteineAnti-Inflammatory AgentsAntioxidantsBiomarkersInterleukin-6MalondialdehydeNeuroprotective AgentsPhosphopyruvate HydrataseS100 Calcium Binding Protein beta SubunitGlasgow Coma ScaleMalondialdehydeN-AcetylcysteineNeuron-specific enolaseS100BTraumatic brain injury

Identifiers

PMID40205270
PMCPMC12213923

What Socratic holds

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Registered trials

None linked

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 Socratic graph.