Your browser doesn't support javascript.
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Añadir filtros

Base de datos
Tipo del documento
Intervalo de año
1.
JAMA Netw Open ; 4(2): e210369, 2021 02 01.
Artículo en Inglés | MEDLINE | ID: covidwho-1084243

RESUMEN

Importance: There is limited evidence regarding early treatment of novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection to mitigate symptom progression. Objective: To examine whether high-dose zinc and/or high-dose ascorbic acid reduce the severity or duration of symptoms compared with usual care among ambulatory patients with SARS-CoV-2 infection. Design, Setting, and Participants: This multicenter, single health system randomized clinical factorial open-label trial enrolled 214 adult patients with a diagnosis of SARS-CoV-2 infection confirmed with a polymerase chain reaction assay who received outpatient care in sites in Ohio and Florida. The trial was conducted from April 27, 2020, to October 14, 2020. Intervention: Patients were randomized in a 1:1:1:1 allocation ratio to receive either 10 days of zinc gluconate (50 mg), ascorbic acid (8000 mg), both agents, or standard of care. Outcomes: The primary end point was the number of days required to reach a 50% reduction in symptoms, including severity of fever, cough, shortness of breath, and fatigue (rated on a 4-point scale for each symptom). Secondary end points included days required to reach a total symptom severity score of 0, cumulative severity score at day 5, hospitalizations, deaths, adjunctive prescribed medications, and adverse effects of the study supplements. Results: A total of 214 patients were randomized, with a mean (SD) age of 45.2 (14.6) years and 132 (61.7%) women. The study was stopped for a low conditional power for benefit with no significant difference among the 4 groups for the primary end point. Patients who received usual care without supplementation achieved a 50% reduction in symptoms at a mean (SD) of 6.7 (4.4) days compared with 5.5 (3.7) days for the ascorbic acid group, 5.9 (4.9) days for the zinc gluconate group, and 5.5 (3.4) days for the group receiving both (overall P = .45). There was no significant difference in secondary outcomes among the treatment groups. Conclusions and Relevance: In this randomized clinical trial of ambulatory patients diagnosed with SARS-CoV-2 infection, treatment with high-dose zinc gluconate, ascorbic acid, or a combination of the 2 supplements did not significantly decrease the duration of symptoms compared with standard of care. Trial Registration: ClinicalTrials.gov Identifier: NCT04342728.


Asunto(s)
Ácido Ascórbico/uso terapéutico , Tratamiento Farmacológico de COVID-19 , Suplementos Dietéticos , Zinc/uso terapéutico , Adulto , Atención Ambulatoria , Antioxidantes/uso terapéutico , COVID-19/complicaciones , Tos/tratamiento farmacológico , Tos/etiología , Disnea/tratamiento farmacológico , Disnea/etiología , Fatiga/tratamiento farmacológico , Fatiga/etiología , Femenino , Fiebre/tratamiento farmacológico , Fiebre/etiología , Gluconatos/uso terapéutico , Humanos , Masculino , Persona de Mediana Edad , SARS-CoV-2 , Índice de Severidad de la Enfermedad , Nivel de Atención , Oligoelementos/uso terapéutico , Resultado del Tratamiento
2.
Cardiovasc Diagn Ther ; 10(4): 912-914, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: covidwho-792582
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA