Frequently Asked Questions
A clinical trial is a research study designed to evaluate new medical treatments, drugs, or devices.
These studies help determine the safety and effectiveness of new therapies before they become widely available.
Clinical trials help advance medical research by testing new treatments that could improve or extend lives.
They are essential in bringing new therapies to patients and ensuring they are safe and effective.
Clinical trials are conducted by medical researchers, doctors, and scientists at hospitals, universities, and clinical research centers.
They are overseen by regulatory authorities like the FDA (U.S.) to ensure patient safety.
Each study has specific eligibility criteria based on factors such as age, medical history, and current health condition.
To see if you qualify, you will need to go through a screening process.
Contact our team for a free pre-screening assessment.
Yes, participation in a clinical trial is completely voluntary. You can withdraw at any time, for any reason, without penalty.
Yes, clinical trials follow strict ethical and regulatory guidelines to ensure patient safety. Before a trial begins, it must be approved by an Institutional Review Board (IRB) to ensure risks are minimized.
All participants are closely monitored, and any side effects are documented. If any serious side effects occur, medical care will be provided, and the study team will adjust the treatment if needed.
No. Clinical trials are designed with patient well-being as the top priority. You will receive high-quality medical care, and your rights and safety are always protected.
No. The sponsor for the clinical trials cover study-related medical visits, treatments, and procedures at no cost to you.
Some clinical trials offer compensation for time and travel. The amount varies depending on the study.
Yes. Your data is protected under HIPAA regulations, and only authorized research staff will have access to your information.
Trial durations vary. Some last a few weeks, while others may continue for months or years. You will be informed about the expected timeline before enrolling.
Yes! You should continue routine care with your primary doctor while participating in the trial.