Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:09 PM
Ignite Modification Date:
2025-12-24 @ 7:09 PM
NCT ID:
NCT02057757
Eligibility Criteria:
Inclusion Criteria:
* Signed informed consent prior to performance or initiation of any study procedures
* Age greater than or equal to 12 months of age (no upper age limit)
* Influenza-like illness (ILI), defined as (all of the following):
* Onset of fever greater than or equal to 38°C (or hypothermia less than 36°C)
* New or worse cough or sore throat
* New or worse shortness of breath or difficulty breathing
* Onset of illness no more than 5 days before screening defined as when the participant experienced at least 1 respiratory symptom, constitutional symptom, or fever
* Hospitalization for ILI (decision for hospitalization will be up to the individual treating clinician), with anticipated hospitalization for more than 24 hours
* One of the following to avoid pregnancy:
* Females who are able to become pregnant (i.e., are not postmenopausal, have not undergone surgical sterilization, and are sexually active with men) must agree to use at least 1 effective form of contraception from the date of informed consent through Day 28 of study
* Males who have not undergone surgical sterilization and are sexually active with women must agree to use condoms or have a partner use at least 1 effective form of contraception through Day 28 of study
Exclusion Criteria:
* Women who are pregnant or breastfeeding
* Clinical suspicion that etiology of illness is primarily bacterial in origin
* Prior treatment with antivirals (e.g., oseltamivir) for the current illness for more than 24 hours
* Unable to take oral medications (adults must tolerate tablets, children must tolerate suspension)
* Unable to tolerate oral food/fluids (absorption is significantly better with food)
* Prior treatment with any investigational drug therapy within 30 days prior to screening
* Known sensitivity to NTZ or any of the excipients comprising the NTZ tablets
* Prior NTZ use within 1 week
* Self-reported history of chronic kidney disease or impaired renal function (no blood or urine kidney function laboratory testing will be done prior to enrollment, but intent is to exclude disease severe enough to cause estimated creatinine clearance \[CrCl\] less than 30)
* Self-reported history of liver disease (no blood laboratory testing will be done prior to enrollment, but intent is to exclude disease severe enough to cause cirrhosis or total bilirubin greater than 2, aspartate aminotransferase \[AST\]/alanine aminotransferase \[ALT\] greater than 3 times the upper limit of normal \[ULN\])
* Presence of any pre-existing illness that, in the opinion of the investigator, would place the participant at an unreasonably increased risk through participation in this study
* Participants who, in the judgment of the investigator, will be unlikely to comply with the requirements of this protocol
* The onset of SARI occurs after hospitalization
* Hospitalized for any reason for greater than 48 hours prior to enrollment
* Participants previously enrolled in this study
* Prior hospital discharge within 30 days
* Known chronic respiratory infection (e.g., tuberculosis, atypical mycobacterial infections)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
12 Months
Study:
NCT02057757
Study Brief:
Protocol Section:
NCT02057757