Anyone can partcipate, regardless of age, sex or ethnicities. Study staff will ensure you meet the inclusion and exclusion criteria outlined in the study protocol.
Clinical Trials are necessary pathway to identify new medical treatments. Your participation in any clinical trial will provide invaluable information whether the particular treatment would be beneficial or not.
For anyone who is interested in participating in a research study, knowledge is important. The Clinical Research Coordinator will provide you with guidelines specified in the protocol to ensure your understanding of the study.
Federally supported and searchable registry for clinical trials pertinence to your condition: www.clinicaltrials.gov
Additional sources include patient advocacy groups.
Simply inform the research team and they will discuss the process of withdrawal from the study.
NO. All study-related assessments are covered by the study budget.
The Institutional Review Board (IRB) will determine the amount and schedule of all payments to participants before the start of the study to ensure that the proposed method and timing will not result in any undue influence as guided by FDA (21 CFR 50.20).