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:
2025-12-25 @ 4:57 AM
Ignite Modification Date:
2025-12-25 @ 4:57 AM
NCT ID:
NCT02644018
Eligibility Criteria:
Inclusion Criteria:
* The informed consent form signed by the patient's parent/adoptive parent to participate in the clinical study.
* Male and female patients aged 3-6.
* Patients with moderate course of influenza or other acute respiratory viral infections.
* Patients with clinically diagnosed influenza or other ARVI based on the body temperature \> 37,5 ° C, not less than 1 of the following other symptoms of intoxication and not less than 1 of the following of catarrhal symptoms:
* Intoxication symptoms: headache, malaise, myalgia, pain in the eyeballs;
* Catarrhal symptoms: sore throat, rhinorrhea, cough, nasal congestion.
* Established diagnosis J06.9, J10, J11, in accordance with ICD-10.
* Uncomplicated course of influenza and other ARVI.
* Interval between onset of symptoms and enrollment to the study of not more than 36 hours.
Exclusion Criteria:
* Complicated course of influenza and other acute respiratory viral infections.
* Treatment with antiviral drugs (antivirals, interferons and interferon inducers), drugs with immunomodulatory effects or antibiotics with systemic and local action within 14 days prior to the screening visit.
* Severe influenza or other ARVI with symptoms of cardiovascular disease, and other symptoms of infectious-toxic shock, and meningoencephalitic syndromes.
* Signs of primary viral pneumonia development (presence of two or more of the following symptoms): shortness of breath, chest pain when coughing, systemic cyanosis, dullness of percussion sound at symmetrical assessment of the upper and lower parts of the lungs.
* Infectious diseases within the last week prior to enrollment.
* "RRI children" (incidence of ARVI within the last 12 months is 6 times or more).
* Asthma history.
* History of increased seizure activity.
* Severe decompensated or unstable medical or psychiatric conditions (any diseases or conditions that threaten the life of the patient or worsen the patient's prognosis and also make it impossible to conduct a clinical study in the patient).
* Cancer, HIV infection, tuberculosis, including those in history.
* Hypersensitivity to imidazolyl ethanamide pentandioic acid and/or excipients of Ingavirin product.
* Diabetes, lactose intolerance, lactase deficiency, glucose-galactose malabsorption, deficiency of sucrase/isomaltase, fructose intolerance, hereditary glucose malabsorption, deficiency of glucose-6-phosphate dehydrogenase.
* Participation of the patient in any other clinical trial within the last 90 days prior to enrollment.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
3 Years
Maximum Age:
6 Years
Study:
NCT02644018
Study Brief:
Protocol Section:
NCT02644018