Current Clinical Trials

Explore the clinical studies currently being conducted at Tapia Research and learn how you may participate in advancing medical innovation.

Available Clinical Trials

Tapia Research is currently conducting clinical trials focused on improving treatments for a variety of health conditions. Explore the studies below to see if you may qualify to participate.

NOW ENROLLING

Cholesterol Study

Cholesterol Study

This clinical study is evaluating potential new treatments designed to help manage high cholesterol levels and improve cardiovascular health.

Eligibility Highlights

  • Adults aged 18 years and older
  • Diagnosed with high cholesterol
  • Not currently participating in another clinical study

NOW ENROLLING)

Thyroid Study

Thyroid Study

This study is focused on evaluating new treatment approaches for individuals experiencing thyroid-related conditions.

Eligibility Highlights

  • Adults with a thyroid condition
  • Available for scheduled visits
  • Meet study requirements

NOW ENROLLING)

Diabetes Study

Diabetes Study

This research study is investigating new therapies that may help improve blood sugar management in individuals living with diabetes.

Eligibility Highlights

  • Adults diagnosed with Type 2 diabetes
  • Stable medication history
  • Meet additional study criteria

What are clinical trials

Clinical trials are research studies that evaluate new medications, treatments, or medical approaches to determine their safety and effectiveness. These studies play a vital role in advancing medical science and improving healthcare for future patients.

By participating in a clinical trial, individuals contribute to the development of innovative therapies while receiving close medical monitoring from experienced research professionals.

The clinical trial process

Participating in a clinical study is a structured and carefully monitored process designed to ensure participant safety and accurate research results.

Screening & Eligibility

Our research team will review your medical history and health information to determine if you qualify for a study.

Enrollment

If eligible, you will receive detailed information about the study and provide informed consent before participation.

Study participation

Participants attend scheduled visits where treatments, tests, and monitoring are conducted according to the study protocol.

Monitoring

Throughout the study, our team closely monitors participant health and collects data to ensure safety and research accuracy.

Your Questions Answered

Are clinical trials safe?

Yes. Clinical trials follow strict regulatory guidelines and ethical standards to ensure participant safety and well-being.

Who cannot participate?

For most clinical studies, if you or your partner are trying to conceive, are currently pregnant, have recently given birth, or are breastfeeding, you may not be eligible to participate. If you use illicit drugs or drink alcohol heavily this may also prevent you from participation.

What will my out-of-pocket cost be?

Neither you nor your insurance will be billed for clinical research participation.

What happens if I no longer wish to participate?

Participation is entirely voluntary. If at any point you wish to stop volunteering for a drug trial at our Paris, TX facility, you may. You will need to contact the site staff to receive any possible necessary steps to ensure your safety.