Are you interested in participating in clinical research?



Clinical Trials Research (CTR) is seeking participants for various clinical studies testing the safety and effectiveness of investigational medications. 


Contributing to research helps people all over the world by providing patients with medical treatments they need to manage their medical condition.


Research participants receive many benefits at no cost including:


  • All study medication
  • Study-related physical exams, procedures, and lab work
  • Compensation for time and travel is provided if you qualify.

 


Please check out our qualification information below and fill out our "Get Started" form to sign up and see if you qualify for this study.


Get Started

Greater Sacramento, California Residents Only
Please fill out the form below and our friendly office staff will connect with you to see if you qualify for this study.

Located outside of California?
Please DO NOT fill out this form. Instead, please visit www.ClinicalTrials.gov to find a study near you. Thank you!


Seeking volunteers for our Clinical Studies

Thank you for considering participation in our clinical study. After filling out the "Get Started" form, a member of our medical team will contact you to obtain more information, answer any questions you have and schedule an appointment for an office visit. In accordance with HIPAA regulations, your personal information will be maintained in strict confidence and will not be sold or used for any other purpose.

Study Length

Varies by study

Qualifications

  • Varies by study

Benefits

Participants will receive the following at no cost:

  • All study medication
  • Study-related physical exams, procedures, and lab work.

Time & Travel

Compensation for time and travel is provided if you qualify.

Our Process

Step 1

Contact Us

Select a study above and submit your contact info to us and we will call you.

Step 2

Phone Screen

During a brief phone call, we will discuss your medical history, your medications and study details.

If you meet initial study requirements, we will schedule a convenient time to visit our office and meet with our study team.

Step 3

Office Visit

At your initial visit, you will be asked to complete a basic registration packet and read the study Informed Consent.

After signing the informed consent, we will perform study specific exams, procedures and lab tests.

View Registration Packet

Step 4

Begin Study

If your results meet the study criteria, you will be invited to complete the study.

Every study differs in the number of visits, timeline and potential compensation provided for time and travel. 

Your Study Coordinator and Investigator will provide all of the details and support you will need.