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 @ 7:18 PM
Ignite Modification Date:
2025-12-24 @ 7:18 PM
NCT ID:
NCT02413203
Eligibility Criteria:
Inclusion Criteria:
* Age between 18 - 50
* Volunteers must be in good health as based on medical history
* All volunteers must be non-smoking and non-pregnant
Exclusion Criteria:
* Subjects with any medical condition, which according to the investigator, may interfere with interpretation of the study results, be indicative of an underlying disease state, or compromise the safety of a potential subject (cancer or history of significant cardiovascular disease (including stroke or TIA), renal, hepatic, gastrointestinal, respiratory, endocrine, metabolic, hematopoietic, or neurological disorders).
* Subjects who have received an experimental drug within 30 days prior to the study
* Subjects who have taken medications at least two weeks prior to the study. Subjects using hormonal birth control, however, will not be an exclusionary criterion.
* Subjects who have taken aspirin or aspirin containing products for at least two weeks prior to the study.
* Subjects who are sensitive or allergic to celecoxib (Celebrex) or its components
* Subjects who have taken any formulation of celecoxib including but not limited to Celebrex, Celebra, Onsenal for at least two weeks prior to the start of the study and throughout the study
* Subjects who have taken acetaminophen, NSAIDs, COX-2 inhibitors (OTC or prescription) for at least two weeks prior to the study.
* Subjects who are consuming any type of tobacco product(s).
* Subjects who consume high doses of antioxidant vitamins daily (vitamin C\> 1000mg, Vitamin E\> 400IU, Beta Carotene\> 1000IU, Vitamin A\> 5000IU, Selenium\> 200mcg, Folic Acid\> 1mg) for the two weeks prior to the start of the study and throughout the study.
* Subjects who consume alcohol, caffeine or high fat food 24 hours prior to the study.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT02413203
Study Brief:
Protocol Section:
NCT02413203