What Should a Volunteer Expect Before and During Clinical Trial Participation?

We will answer all your questions, and upon you request, we will discuss it with your partner, family members, and/or your doctors. All our physicians overseeing protocol conduction are board certified and our study staff is highly experienced and well trained.

  • You and your safety are our #1 priority
  • Your doctor will NEVER recommend participation in a protocol that will not be on your BEST interest
  • Participating in research is 100% voluntary. You can withdraw at any time.
  • No discriminations on the bases of age, race, sexual orientation, gender identification, or financial income.
  • Study participation is strictly confidential (tests and procedures results do not have your personal information)
  • Access to free medications, labs, and other special tests usually not covered by insurance companies. There is no cost to you to participate.
  • Stipend or compensation for time and or transportation is usually provided
  • The length of the protocol visits is variable for each study (usually from 15 minutes to 1 hour)
  • Early, flexible, convenient and timely appointments available (average waiting time for a research visit appointments is less than 5 minutes)
  • Protocol visits are mostly conducted on 3rd floor, while our medical clinic is located on the 2nd floor)
  • Compassionate, knowledgeable, friendly staff
  • Linkage to care after the trial if needed

Source: https://clinicaltrials.gov

Ongoing Clinical Research (Click Here)

Clinical Trial Inquiry

To schedule an appointment with one of our board certified specialists call
(407) 647-3960 or click here to request an appointment.