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 @ 9:54 PM
Ignite Modification Date:
2025-12-24 @ 9:54 PM
NCT ID:
NCT01070732
Eligibility Criteria:
Inclusion Criteria:
* Age greater than or equal to 18 years
* Written informed consent by the patients
* Medical condition necessitating the administration of antipyretic or analgesic medications
Exclusion Criteria:
* Αge lower than 18 years
* Lack of informed consent
* History of liver cirrhosis
* Blood creatinine greater than 3mg/dl
* Blood AST greater than 3 times the upper normal level according to the lab of the participating hospital
* History of hypersensitivity to non-steroidal ant-inflammatory drugs
* History of abuse of analgesics
* Pregnancy or lactation
* Fulminant hemorrhage of the upper or lower digestive tract
* Thrombocytopenia defined as less than 50000 platelets/μl
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01070732
Study Brief:
Protocol Section:
NCT01070732