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Efficacy of N-acetyl Cysteine in Severe COVID-19 Patients: A Randomized Controlled Phase III Clinical Trial
Jundishapur Journal of Natural Pharmaceutical Products ; 18(1) (no pagination), 2023.
Article in English | EMBASE | ID: covidwho-2302219
ABSTRACT

Background:

Today, various drugs have been investigated as the primary or complementary treatment for coronavirus disease 2019 (COVID-19). N-acetylcysteine (NAC) has been used as a mucolytic in pulmonary diseases. This drug apparently contributes to the retrieval of the intracellular antioxidant system. Objective(s) This study aimed to determine the efficacy of NAC in severe COVID-19 patients admitted to the intensive care unit (ICU). Method(s) This single-blinded randomized controlled phase III clinical trial included 40 patients with confirmed COVID-19 (based on polymerase chain reaction) admitted to the Shahid Mohammadi Hospital's ICU, Bandar Abbas, Iran, in 2020. All cases had severe COVID-19. They were allocated randomly to two equal groups. Patients in the control group received standard drug therapy based on the treatment protocol of the national COVID-19 committee, while those in the NAC group received a single dose of intravenous NAC (300 mg/kg) upon admission to the ICU in addition to standard drug treatment. Clinical status and laboratory tests were done on admission to the ICU and then 14 days later or at discharge without knowing the patient grouping. Result(s) The two groups were comparable regarding age, gender, and other baseline laboratory and clinical parameters. At the final evaluation, respiratory rate (21.25 +/- 4.67 vs. 27.37 +/- 6.99 /min) and D-dimer (186.37 +/- 410.23 vs. 1339.04 +/- 2183.87 ng/mL) were significantly lower in the NAC group (P = 0.004 and P = 0.030, respectively). Also, a lower percentage of patients in the NAC group had lactate dehydrogenase (LDH) <= 245 U/L (0% vs. 25%, P = 0.047). Although the length of ward and ICU stay was shorter in the NAC group than in controls, the difference was statistically insignificant (P = 0.598 and P = 0.629, respectively). Mortality, on the other hand, was 75% in the control group and 50% in the NAC group, with no statistically significant difference (P = 0.102). Concerning the change in the study parameters, only the decrease in diastolic blood pressure (DBP) was significantly higher with NAC (P = 0.042). The intubation and mechanical ventilation rates were higher, while oxygen with mask and nasal oxygen rates were lower with NAC, but the difference was statistically insignificant. Conclusion(s) Based on the current research, NAC is related to a significant decrease in RR, D-dimer, and DBP in severe COVID-19. Also, LDH was significantly lower in the NAC group than in the controls. More research with larger sample sizes is needed to validate the current study results.Copyright © 2023, Author(s).
Keywords
Efficacy; N-acetylcysteine; Severe COVID-19; adult; article; artificial ventilation; blood pH; body temperature; breathing rate; carbon dioxide tension; clinical article; controlled study; coronavirus disease 2019/dt [Drug Therapy]; coronavirus disease 2019/th [Therapy]; diastolic blood pressure; drug efficacy; erythrocyte sedimentation rate; female; human; intensive care unit; international normalized ratio; intubation; laboratory test; length of stay; leukocyte count; lymphocyte count; lymphocyte percentage; male; mask ventilation; middle aged; mortality rate; neutrophil count; neutrophil percentage; oxygen saturation; parallel design; partial thromboplastin time; phase 3 clinical trial; platelet count; polymerase chain reaction; randomized controlled trial; red blood cell distribution width; single blind procedure; single drug dose; systolic blood pressure; urea nitrogen blood level; acetylcysteine/ct [Clinical Trial]; acetylcysteine/dt [Drug Therapy]; acetylcysteine/iv [Intravenous Drug Administration]; alanine aminotransferase/ec [Endogenous Compound]; alkaline phosphatase/ec [Endogenous Compound]; aspartate aminotransferase/ec [Endogenous Compound]; atazanavir/dt [Drug Therapy]; atazanavir plus ritonavir/dt [Drug Therapy]; bilirubin/ec [Endogenous Compound]; bilirubin glucuronide/ec [Endogenous Compound]; C reactive protein/ec [Endogenous Compound]; calcium/ec [Endogenous Compound]; chloroquine/cb [Drug Combination]; chloroquine/dt [Drug Therapy]; creatinine/ec [Endogenous Compound]; D dimer/ec [Endogenous Compound]; ferritin/ec [Endogenous Compound]; hydroxychloroquine sulfate/cb [Drug Combination]; hydroxychloroquine sulfate/dt [Drug Therapy]; lactate dehydrogenase/ec [Endogenous Compound]; lopinavir plus ritonavir/dt [Drug Therapy]; phosphorus/ec [Endogenous Compound]; oxygen mask

Full text: Available Collection: Databases of international organizations Database: EMBASE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Journal: Jundishapur Journal of Natural Pharmaceutical Products Year: 2023 Document Type: Article

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Full text: Available Collection: Databases of international organizations Database: EMBASE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Journal: Jundishapur Journal of Natural Pharmaceutical Products Year: 2023 Document Type: Article