Selected article for: "exact test and experimental group"

Author: Di Domênico, Marielle Bazzo; Cesca, Henrique; Ponciano, Thales Henrique Jincziwski; dos Santos, Renan Brandenburg; Lenz, Ulysses; Antunes, Vinícius Picoli; Godinho, Vinicius Webber; Collares, Kauê; Corazza, Pedro Henrique
Title: Effectiveness of hydrogen peroxide as auxiliary treatment for hospitalized COVID-19 patients in Brazil: preliminary results of a randomized double-blind clinical trial
  • Cord-id: a7gf48y2
  • Document date: 2021_5_1
  • ID: a7gf48y2
    Snippet: OBJECTIVES: To evaluate the effectiveness of hydrogen peroxide (H(2)O(2)) in the form of mouthwash and nasal spray as an auxiliary treatment for coronavirus disease 2019 (COVID-19). METHODS: Forty hospitalized patients who tested positive for severe acute respiratory syndrome coronavirus 2 using a reverse-transcription polymerase chain reaction test were evaluated. They were randomly divided into an experimental group (n= 20; gargling with 1.0% H(2)O(2) and nasal wash with 0.5% H(2)O(2)) or a co
    Document: OBJECTIVES: To evaluate the effectiveness of hydrogen peroxide (H(2)O(2)) in the form of mouthwash and nasal spray as an auxiliary treatment for coronavirus disease 2019 (COVID-19). METHODS: Forty hospitalized patients who tested positive for severe acute respiratory syndrome coronavirus 2 using a reverse-transcription polymerase chain reaction test were evaluated. They were randomly divided into an experimental group (n= 20; gargling with 1.0% H(2)O(2) and nasal wash with 0.5% H(2)O(2)) or a control group (n= 20). The solutions were used for 7 days and the patients were monitored every 2 days, for a total of 8 days. At check-ups, patients were asked about their symptoms and possible adverse effects of the solutions. The presence and severity (mild, moderate, or severe) of symptoms were recorded. Data were compared using the Student test and the Fisher exact test (α= 0.05). RESULTS: There was no significant difference between the 2 groups in the length of hospital stay (p= 0.65). The most frequent symptom on day 0 was coughing (72.0% in the experimental group and 76.5% in the control group), which abated over time. There was no significant difference between the groups in the evaluated symptoms. Most (75.0%) of the patients in the experimental group presented a reduction in dyspnea between days 0 and 2. Few patients reported adverse effects from the use of the solutions. CONCLUSIONS: H(2)O(2) as a mouthwash and nasal spray is safe to use. There is insufficient evidence to demonstrate that H(2)O(2) is effective as an auxiliary treatment for hospitalized COVID-19 patients.

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