Selected article for: "primary endpoint and viral load"

Author: Pott-Junior, Henrique; Bastos Paoliello, Mônica Maria; Miguel, Alice de Queiroz Constantino; da Cunha, Anderson Ferreira; de Melo Freire, Caio Cesar; Neves, Fábio Fernandes; da Silva de Avó, Lucimar Retto; Roscani, Meliza Goi; dos Santos, Sigrid De Sousa; Chachá, Silvana Gama Florêncio
Title: Use of ivermectin in the treatment of Covid-19: A pilot trial
  • Cord-id: fub50lvt
  • Document date: 2021_3_9
  • ID: fub50lvt
    Snippet: OBJECTIVES: In this randomized open-label trial pilot study we assessed the antiviral effects and safety of various doses of ivermectin in patients with mild clinical symptoms of COVID-19. METHODS: Patients were randomly assigned to receive standard of care (SOC) treatment at hospital admission; SOC plus ivermectin 100 mcg/kg; SOC plus ivermectin 200 mcg/kg; or SOC plus ivermectin 400 mcg/kg. The primary assessed endpoint was the proportion of patients who achieved two consecutive negative SARS-
    Document: OBJECTIVES: In this randomized open-label trial pilot study we assessed the antiviral effects and safety of various doses of ivermectin in patients with mild clinical symptoms of COVID-19. METHODS: Patients were randomly assigned to receive standard of care (SOC) treatment at hospital admission; SOC plus ivermectin 100 mcg/kg; SOC plus ivermectin 200 mcg/kg; or SOC plus ivermectin 400 mcg/kg. The primary assessed endpoint was the proportion of patients who achieved two consecutive negative SARS-CoV-2 RT PCR tests within 7 days of the start of the dosing period. This study was registered at ClinicalTrials.gov (NCT04431466). RESULTS: A total of 32 patients were enrolled and randomized to treatment. SOC treatment together with ivermectin did not result in any serious adverse events. All patients exhibited a reduction in SARS-CoV-2 viral load within 7 days; however, those who received ivermectin had a more consistent decrease as compared to the SOC alone group, characterized by a shorter time for obtaining two consecutive negative SARS-CoV-2 RT PCR tests. CONCLUSIONS: Ivermectin is safe in patients with SARS-CoV-2, reducing symptomatology and the SARS-CoV-2 viral load. This antiviral effect appears to depend on the dose used, and if confirmed in future studies, it suggests that ivermectin may be a useful adjuvant to the SOC treatment in patients with mild COVID-19 symptoms.

    Search related documents:
    Co phrase search for related documents
    • abdominal pain and adjusted odds: 1, 2, 3, 4, 5
    • abdominal pain and adjusted odds ratio: 1, 2, 3, 4, 5
    • add therapy and additional study: 1, 2
    • additional study and adjusted odds: 1, 2, 3, 4, 5, 6, 7
    • additional study and adjusted odds ratio: 1, 2, 3, 4, 5