Created at Source Raw Value Validated value
March 13, 2021, 12:31 a.m. usa

inclusion criteria: - covid-19 positive by polymerase chain reaction (pcr) testing; - participant must be able to evaluate their symptoms and report them in the symptoms diary; - patients must be able to take their oral temperature daily with an electronic thermometer provided to them with study materials; - males and females, at least 18 years of age, capable and willing to provide informed consent; - female patient is either not of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile, or is of childbearing potential and practicing at least one method of contraception and preferably two complementary forms of contraception including a barrier method (e.g. male or female condoms, spermicides, sponges, foams, jellies, diaphragm, intrauterine device (iud)) throughout the study; - patient must have received a diagnosis of covid-19 infection within the last 48 hours and have one or more symptoms; - outpatient setting (not currently hospitalized or under immediate consideration for hospitalization); - patient must be able and willing to comply with the requirements of this study protocol.

inclusion criteria: - covid-19 positive by polymerase chain reaction (pcr) testing; - participant must be able to evaluate their symptoms and report them in the symptoms diary; - patients must be able to take their oral temperature daily with an electronic thermometer provided to them with study materials; - males and females, at least 18 years of age, capable and willing to provide informed consent; - female patient is either not of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile, or is of childbearing potential and practicing at least one method of contraception and preferably two complementary forms of contraception including a barrier method (e.g. male or female condoms, spermicides, sponges, foams, jellies, diaphragm, intrauterine device (iud)) throughout the study; - patient must have received a diagnosis of covid-19 infection within the last 48 hours and have one or more symptoms; - outpatient setting (not currently hospitalized or under immediate consideration for hospitalization); - patient must be able and willing to comply with the requirements of this study protocol.

Jan. 29, 2021, 12:31 a.m. usa

inclusion criteria: - covid-19 positive by polymerase chain reaction (pcr) testing or by confirmed epidemiological link (as defined by public health services at the time of inclusion); - participant must be able to evaluate their symptoms and report them in the symptoms diary; - patients must be able to take their oral temperature daily with an electronic thermometer provided to them with study materials; - males and females, at least 18 years of age, capable and willing to provide informed consent; - female patient is either not of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile, or is of childbearing potential and practicing at least one method of contraception and preferably two complementary forms of contraception including a barrier method (e.g. male or female condoms, spermicides, sponges, foams, jellies, diaphragm, intrauterine device (iud)) throughout the study; - patient must have received a diagnosis of covid-19 infection within the last 48 hours and have one or more symptoms; - outpatient setting (not currently hospitalized or under immediate consideration for hospitalization); - patient must be able and willing to comply with the requirements of this study protocol.

inclusion criteria: - covid-19 positive by polymerase chain reaction (pcr) testing or by confirmed epidemiological link (as defined by public health services at the time of inclusion); - participant must be able to evaluate their symptoms and report them in the symptoms diary; - patients must be able to take their oral temperature daily with an electronic thermometer provided to them with study materials; - males and females, at least 18 years of age, capable and willing to provide informed consent; - female patient is either not of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile, or is of childbearing potential and practicing at least one method of contraception and preferably two complementary forms of contraception including a barrier method (e.g. male or female condoms, spermicides, sponges, foams, jellies, diaphragm, intrauterine device (iud)) throughout the study; - patient must have received a diagnosis of covid-19 infection within the last 48 hours and have one or more symptoms; - outpatient setting (not currently hospitalized or under immediate consideration for hospitalization); - patient must be able and willing to comply with the requirements of this study protocol.