Anyone who meets the study requirements, known as eligibility criteria, may be eligible to participate. These criteria help ensure the research is safe and that the results are accurate.
Eligibility may be based on:
Eligibility depends on the study design and safety requirements. Researchers use eligibility criteria to protect participants and ensure reliable results.
Common eligibility factors include:
Participation usually begins with a screening visit to confirm eligibility. If eligible, participants attend scheduled visits where researchers collect information and monitor health.
Activities may include:
Tests depend on the study and its goals. They are designed to monitor safety and measure how the treatment works.
Common tests may include:
After the trial ends, researchers review the results and continue monitoring participant safety if required.
Participants may:
Participant safety is monitored by multiple independent groups throughout the study.
These may include:
Clinical trials must be designed and monitored to ensure participants are protected and risks are carefully managed.
Participants are typically reimbursed for their time and travel expenses.
Reimbursement helps cover:
The amount and schedule are explained before participation begins.
After you register, our team will review your information and contact you to discuss the study.
The next steps may include:
This process helps confirm whether the study is suitable and safe for you.
If you are eligible and choose to proceed, we will schedule your first study visit.
Access to your information is limited to authorised people who need it to run and monitor the study.
This may include:
All organisations must follow strict privacy and confidentiality rules.
Yes. You can request to withdraw your consent for the use of your information at any time.
If you withdraw from a study:
Withdrawing will not affect your medical care.
