Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
The University of Texas Health Science Center at San Antonio
Age
18–any
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
At least 18 years of age
Post-menopausal as confirmed by medical history
Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's IRB/Ethics Committee
You may not be if
Evidence of active cancer (patients with a prior history of malignancy are encouraged to participate, but due to cytokine levels associated with malignancy there must be no evidence of disease)
Cachexia
Active systemic illness (infection including viral illnesses such as Hepatitis and HIV)
Chronic use of aspirin of omega-3 free fatty acid supplementation within the last 60 days (defined as greater than or equal to 7 consecutive days)
Known hypersensitivity to aspirin and/or omega-3 fatty acids
Actively receiving a physician-directed regimen of aspirin and/or receiving herapeutic/prophylactic anticoagulation
Any aspirin or omega-3 free fatty acid supplementation within the last 14 days
Subjects who are pregnant
History of medical noncompliance
Clareo Health | Impact of COX2 on Sera Biomarkers From Obese Subjects
