(708) 773-0082
Axis Clinical Research

For Patients

Everything you need to know about participating in clinical research — in plain language.

What is a clinical trial?

A clinical trial is a carefully monitored research study that helps determine whether a new treatment is safe and effective. Every medication in your pharmacy exists because people chose to participate in one. Trials follow strict protocols, are overseen by independent ethics boards, and are conducted by trained medical professionals.

Who can participate?

Each study has specific criteria — age, diagnosis, current medications, and health history. That is what our free screening process is for: a short call with our team, then a no-cost screening visit where our medical staff confirms whether a study is right for you. If one study is not a fit, another might be.

What should I expect?

Clear communication, first. Before anything begins you receive a full explanation of the study — its purpose, schedule, procedures, and compensation — in writing, with time to ask questions. During the study you attend scheduled visits where our team monitors your health closely, often more closely than routine care.

Your rights as a participant

  • Be fully informed about the study before you agree to anything
  • Ask questions at any time — and get clear answers
  • Withdraw at any point, for any reason, without penalty
  • Have your privacy protected under HIPAA at every step
  • Receive study-related medical care at no cost
  • Be told about any new findings that might affect your willingness to continue

Frequently Asked Questions

Does it cost anything to participate?+

No. All study-related visits, tests, procedures, and study medication are provided at no cost. You never need insurance, and we never ask for payment information.

Will I be paid?+

Yes — participants are compensated for their time and travel at each completed visit. The amount varies by study and is explained clearly before you enroll.

Is it safe?+

Every study we run is reviewed and approved by an Institutional Review Board (IRB) — an independent ethics committee — and conducted under FDA regulations. Your safety is monitored at every visit.

Can I quit if I change my mind?+

Always. Participation is completely voluntary and you can withdraw at any time, for any reason, without penalty and without affecting your regular medical care.

Will my information stay private?+

Yes. Your health information is protected under HIPAA and handled according to strict confidentiality rules. Study data is coded and never shared with your name attached.

What if I do not qualify for one study?+

We screen every patient against all of our active and upcoming studies. If one is not a fit, another may be — and we keep you in mind as new studies open.

📞 Call (708) 773-0082 — Coordinators Available