Painful nerve damage to your feet and legs from diabetes?

Diabetic peripheral neuropathy (DPN) is a complication of diabetes that results in nerve damage to your feet and legs. 


Clinical Trials Research® (CTR) often has clinical studies seeking individuals suffering from painful diabetic peripheral neuropathy (DPN). These studies typically are designed to potentially relieve the pain caused by this condition.


Please check out our qualification information below and fill out our "Get Started" form to sign up and see if we are currently offering a study for DPN and if so, to 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 with Diabetic Peripheral Neuropathy (DPN)

Thank you for considering participation in our Diabetic Peripheral Neuropathy (DPN) studies. 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

  • At least 18 years of age.
  • Diagnosed with type 1 or 2 diabetes. 
  • Do not have unstable diabetes or significant medical problems
  • Have a documented diagnoses of bilateral painful diabetic peripheral neuropathy in both lower extremities.


Benefits

Participants will receive the following at no cost: all study-related medical care, physical exams, procedures, and lab work.

Time & Travel

Compensation for time and travel may be provided if you qualify.

Our Process

Step 1

Contact Us

Fill out the "Get Started" form 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.