Frequently Asked Questions

A clinical trial is a research study in which volunteer participants help researchers evaluate the safety and effectiveness of new medical treatments, medications, or devices. All trials conducted through Peak Clinical are regulated by the FDA and reviewed by an independent Institutional Review Board (IRB).

Participant safety is our highest priority. All studies undergo rigorous review before enrolling participants, and safety is monitored throughout the duration of every study. You will be fully informed of any known risks before agreeing to participate, and you can withdraw at any time without explanation.

No. Study-related visits, examinations, and investigational treatments are provided at no cost to participants. Many studies also offer financial compensation for your time and travel expenses.

A member of our research team will review your information and reach out — typically within 1–2 business days — to discuss whether there are currently enrolling studies near you that may be appropriate for your situation. No commitment is required at that stage.

Yes. Participation in any clinical trial is completely voluntary. You may withdraw at any time, without explanation, and without any effect on your regular medical care or relationship with your physician.

Your information is used solely to determine potential study eligibility and to contact you about research opportunities. We do not sell, rent, or share your information with third parties or affiliate marketers. Please see our Privacy Policy for full details.

Some studies do use placebos as a comparison. If a study involves a placebo, this will be fully explained before you consent to participate. You will always know the possibility of receiving a placebo before agreeing to enroll in any study.

Study duration varies widely depending on the therapeutic area and phase of the trial. Some studies require a single visit while others may involve regular check-ins over several months. The full schedule and time commitment will be explained clearly before you decide to enroll.

All participants have access to the study medical team throughout the duration of the trial. Any adverse event or side effect is documented, reported, and addressed promptly. Your safety and wellbeing are always the top priority.

No referral is needed. You can submit your information directly through our intake form and our team will guide you through the eligibility process. However, we always encourage you to keep your primary care provider informed of your participation in any study.