A clinical trial is a research study that tests new medications, treatments, or medical devices in volunteer participants. Before reaching this stage, treatments undergo years of laboratory and preclinical testing. Clinical trials are the final step before a treatment can be made available to the public.
At CRP, we conduct Phase 2 through Phase 4 trials across cardiology, dermatology, endocrinology, neurology, rheumatology, and more. Each trial follows a detailed plan called a protocol, and every participant is closely monitored by our medical team throughout the study.
Each study has specific eligibility criteria based on age, medical history, current medications, and the condition being studied. Some studies are open to healthy volunteers, while others require a specific diagnosis such as Type 2 diabetes, high cholesterol, or eczema.
The best way to find out if you qualify is to browse our active studies or call us at (215) 676-6696. Our team will walk you through the screening process over the phone before you ever come in for a visit.
Your safety is our top priority. Every clinical trial at CRP is:
That said, investigational treatments may have unknown side effects, and there is no guarantee the treatment will work for you. The informed consent process ensures you fully understand the potential risks and benefits before you decide to participate. You can withdraw from any study at any time for any reason.
Before your first visit, our team conducts a pre-screening phone call to review your medical history and confirm you may be eligible. If you are a potential fit, we schedule a screening visit at our facility.
During the screening visit, you will:
Screening visits typically take 2-4 hours. Follow-up visits are usually 1-2 hours. Learn more on our How It Works page.
Informed consent is a conversation between you and the study team, not just a form to sign. Before enrolling, we explain:
You are encouraged to ask questions and take time to decide. You may also discuss the study with your family or personal physician before making a decision.
Yes. Participation is completely voluntary. You can withdraw from any study at any time, for any reason, with no penalty and no impact on your regular medical care. If you decide to leave, our team will ensure a safe transition and communicate any relevant findings to your primary care physician if you wish.
Yes. Most CRP studies offer compensation for your time and travel. Payment is provided after each completed visit via a reloadable Visa debit card.
The amount varies by study and depends on the complexity of procedures, visit duration, and number of visits required. You can ask about specific compensation during your first phone call with our team.
In addition, all study-related medical care, lab work, and medications are provided at no cost to you.
CRP has two locations:
For qualifying studies, CRP provides free Lyft rides to and from your appointments. Your study coordinator arranges transportation for you -- no reimbursement forms or out-of-pocket costs.
No. All study-related procedures, lab work, medications, and physician visits are paid for by the study sponsor. Your insurance is not billed for any study-related care. You do not need health insurance to participate in a clinical trial at CRP.
Only if you choose. At the end of a study, CRP can send a follow-up letter to your primary care physician summarizing your participation and any relevant findings. This is entirely optional and requires your consent.
Yes. Your personal and medical information is protected under strict HIPAA privacy and security standards. All clinical trial data is de-identified before being shared with study sponsors. Your name and personal details are never included in published research results.
Read our full Privacy Policy for details on how we collect, use, and protect your information.
We are here to help. You can reach our team by:
Our recruiters are available Monday through Friday, 8:00 AM to 5:00 PM, and are happy to answer any questions about our studies or the enrollment process.