Protecting the safety, rights, and well-being of research participants is our highest priority. Every clinical research study conducted at Gastro Health follows strict ethical, scientific, and regulatory standards.
Independent Ethics Review
Before a study can begin, it must be reviewed and approved by an independent Institutional Review Board (IRB). The IRB evaluates:
- Participant safety
- Potential risks and benefits
- Patient rights
- Study procedures
- Informed consent documents
Studies cannot proceed without IRB approval.
Informed Consent
Participation in clinical research is always voluntary. Before joining a study, you will receive detailed information about what participation involves and will have the opportunity to ask questions. You may choose not to participate or withdraw from a study at any time.
Ongoing Safety Monitoring
Throughout the study, participants are monitored by:
- Physician investigators
- Research coordinators
- Study sponsors
- Independent safety committees, when applicable
Any new information that may affect your decision to participate will be shared with you promptly.
Privacy and Confidentiality
Gastro Health is committed to protecting your personal health information. Research records are maintained according to applicable privacy laws, regulatory requirements, and industry standards designed to safeguard participant confidentiality.
Your Rights as a Research Participant
As a research participant, you have important rights.
You have the right to:
- Receive information about the study before making a decision
- Ask questions at any time
- Understand potential risks and benefits
- Take time to consider participation
- Discuss participation with family or healthcare providers
- Decline participation without affecting your medical care
- Withdraw from a study at any time
Our research team is committed to ensuring that every participant feels informed, respected, and supported throughout the research process.