Selected article for: "fever duration and primary outcome"

Author: Shahbaznejad, Leila; Davoudi, Alireza; Eslami, Gohar; Markowitz, John S.; Navaeifar, Mohammad Reza; Hosseinzadeh, Fatemeh; Movahedi, Faeze Sadat; Rezai, Mohammad Sadegh
Title: Effect of ivermectin on COVID-19: A multicenter double-blind randomized controlled clinical trial
  • Cord-id: rh2jrojk
  • Document date: 2021_5_6
  • ID: rh2jrojk
    Snippet: PURPOSE: : Given the coronavirus disease-2019 (COVID-19) pandemic, there is a global urgency to discover an effective treatment against this disease. This study aimed to evaluate the effect of the widely used antiparasitic drug ivermectin on COVID-19 patient outcomes. METHODS: In this randomized double-blind clinical trial, COVID-19 patients admitted to two referral tertiary hospitals of Mazandaran, north of Iran, were randomly divided into two groups of intervention and control. In addition to
    Document: PURPOSE: : Given the coronavirus disease-2019 (COVID-19) pandemic, there is a global urgency to discover an effective treatment against this disease. This study aimed to evaluate the effect of the widely used antiparasitic drug ivermectin on COVID-19 patient outcomes. METHODS: In this randomized double-blind clinical trial, COVID-19 patients admitted to two referral tertiary hospitals of Mazandaran, north of Iran, were randomly divided into two groups of intervention and control. In addition to standard treatment for COVID-19, the intervention group received a single weight-based dose (0.2 mg/kg) of ivermectin. Demographic, clinical, laboratory and imaging data of participants were recorded at baseline. Patients were daily assessed for clinical complaints and disease progression. The primary clinical outcome measures were duration of hospital stay, fever, dyspnea, cough, and overall clinical improvement. FINDINGS: : Sixty-nine patients with the mean age of 47.6±22.2 and 45.2±23.1 years participated in intervention and control groups, respectively (p=0.6). Nineteen patients (54%) in the ivermectin group and 18(53%) in control group were male (p=0.9). The mean duration of dyspnea was 2.4±1.7 days in the ivermectin and 3.7±2.1 days in the control group (p=0.02). Also, persistent cough lasted for 3.1±1.9 days in the ivermectin group compared to 4.8±2.0 days in control group (p=0.00). The mean duration of hospital stay was 6.9±3.1 vs 8.3±3.3 days for the ivermectin and control group, respectively (p=0.01). Also, the frequency of lymphopenia decreased to 14.3% in the ivermectin group and did not change in the control group (p=0.00). IMPLICATIONS: A single dose of ivermectin was well-tolerated in symptomatic COVID-19 patients and improved important clinical features of COVID-19 patients including dyspnea, cough, and lymphopenia. Further studies with larger sample sizes, different drug dosages, dosing intervals and durations, especially in different stages of the disease, may help understanding ivermectin's potential clinical benefits. TRIAL REGISTRATION: The current controlled trial was registered in the Iranian Registry of Clinical Trials (code: IRCT20111224008507N3) on 2020-06-27.

    Search related documents:
    Co phrase search for related documents
    • abdominal pain and admission dyspnea: 1, 2, 3
    • abdominal pain and admission time: 1, 2, 3, 4, 5, 6, 7
    • abdominal pain and lopinavir ritonavir: 1, 2, 3, 4
    • abdominal pain and lopinavir ritonavir hydroxychloroquine: 1, 2
    • abdominal pain and low lymphocyte: 1, 2, 3
    • abdominal pain and low lymphocyte count: 1, 2
    • abdominal pain and lung tissue: 1, 2
    • adequate efficacy and admission time: 1
    • admission day and lopinavir ritonavir: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15
    • admission day and lopinavir ritonavir hydroxychloroquine: 1, 2, 3, 4, 5
    • admission day and lopinavir ritonavir hydroxychloroquine antibiotic: 1
    • admission day and low lymphocyte: 1, 2, 3, 4
    • admission day and low lymphocyte count: 1, 2, 3
    • admission day and lung tissue: 1, 2
    • admission dyspnea and lopinavir ritonavir: 1, 2
    • admission time and lopinavir ritonavir hydroxychloroquine: 1, 2, 3, 4, 5, 6, 7
    • admission time and low lymphocyte: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10
    • admission time and low lymphocyte count: 1, 2, 3, 4, 5, 6
    • admission time and lung tissue: 1