Skip to main content
5927 Webb Rd Tampa FL 33615 (813) 249-9100
Enroll Today
Santos Research Center, Corp.

Paid Clinical Trials in Tampa

Browse paid clinical trials in Tampa and explore current studies by condition. Compensation may be available depending on the study.

  • Compensation for time and travel
  • No insurance required
  • No-cost study-related care
  • Transportation assistance available
  • FDA- and IRB-approved research
See If You Qualify Call (813) 249-9100

Currently Enrolling Paid Clinical Trials in Tampa

Explore clinical trials currently enrolling at Santos Research Center in Tampa. Browse studies by condition and learn more about eligibility, participation requirements, and available research opportunities.

New study available

Ulcerative Colitis Clinical Trial

This study is evaluating an investigational enema for adults with active ulcerative colitis affecting the left side of the colon.

Diagnosis

Mild to moderately active left-sided ulcerative colitis, confirmed through medical evaluation.

Age

18 to 65 years.

Treatment history

Symptoms have continued despite treatment, or a previous treatment was not tolerated.

Participation

A daily enema for 28 days and approximately 9 study visits over 10 weeks. Participants may receive the investigational treatment or a placebo.

Exclusions

Severe or more extensive colitis, Crohn’s disease, certain infections, or pregnancy or breastfeeding.

The study team will review the full criteria during screening.

Clinical research coordinator consulting with an adult participant

New study available

Narcolepsy Clinical Trial

This study is evaluating an investigational medication for adults with narcolepsy type 1 or type 2.

Diagnosis

Participants must have a confirmed diagnosis of narcolepsy type 1 or type 2.

Age

Participants must be at least 18 years old.

Daytime sleepiness

Participants must have significant daytime sleepiness. Those with type 1 must also have at least 4 cataplexy episodes per week.

Sleep schedule

Participants should generally keep a regular sleep schedule and spend 7 to 9 hours in bed each night.

Participation

Approximately 14 weeks of treatment, followed by 2 weeks of follow-up. Participants may receive the investigational medication or a placebo.

Exclusions

Pregnancy, moderate to severe sleep apnea, and certain medical conditions. Some narcolepsy and sleep medications require review before participation.

The study team will review the full criteria during screening.

Adult participant discussing sleep history with a clinical research professional

New study available

High Blood Pressure Clinical Trial

This study is evaluating an investigational medication added to usual blood pressure treatment in people with uncontrolled hypertension and cardiovascular disease or a high risk of developing it.

Diagnosis

Blood pressure must remain elevated at screening despite treatment.

Age

18 or older with established cardiovascular disease, or 55 or older with multiple cardiovascular risk factors.

Heart health

Qualifying conditions may include a prior heart attack, stroke, or peripheral artery disease. Other patients may qualify based on a combination of risk factors.

Current treatment

Participants must be taking stable blood pressure medications, including a diuretic and at least one other medication.

Exclusions

A recent heart attack or stroke, certain kidney or potassium test results, or pregnancy or breastfeeding.

The study team will review the full criteria during screening.

Clinical research professional checking an adult participant’s blood pressure

New study available

COPD Clinical Trial

This study is evaluating an investigational treatment for adults with COPD and type 2 inflammation.

Diagnosis

This study is for adults with COPD and type 2 inflammation.

COPD treatment

Participants should generally have used three types of maintenance inhaler medication for at least 6 months.

Study treatment

Participants may receive the investigational treatment or a placebo.

Recent symptoms

A COPD flare, pneumonia, or lower respiratory infection within 4 weeks before screening may exclude participation.

Exclusions

People with a current or previous physician diagnosis of asthma are excluded. Needing oxygen for more than 16 hours a day or having certain other significant lung conditions may also exclude participation.

The study team will review the full criteria during screening.

Adult participant and clinical research professional discussing a lung model

New study available

RSV Clinical Trial

This study is evaluating an investigational treatment for adults with RSV who are at higher risk of severe illness.

Diagnosis

An RSV test must confirm the infection.

Age

Participants must be at least 18 years old.

Recent symptoms

A new or worsening symptom, such as cough, fever, congestion, or shortness of breath, must have started within the past 72 hours.

Higher risk

Participants must be at least 75 years old or have a qualifying chronic lung or heart condition that causes symptoms and requires ongoing treatment.

Exclusions

People who are hospitalized or expected to be hospitalized within 24 hours, or who are immunocompromised, may not qualify. Female participants must also meet the study’s reproductive eligibility requirements.

The study team will review the full criteria during screening.

Older adult participant discussing study screening with a clinical research professional

Study availability may change throughout the year based on sponsor requirements and enrollment status.

Types of Clinical Trials

Clinical trials may focus on different research goals depending on the treatment, condition, or health question being studied.

Treatment trials

Test medications, therapies, devices, or other medical approaches.

Prevention trials

Study ways to reduce the risk of certain conditions.

Screening trials

Look for better ways to detect health conditions earlier.

Genetic studies

Explore how genes may relate to disease risk or treatment response.

Quality of life trials

Focus on comfort, daily function, and long-term care needs.

For more detail, read our guide to types of clinical trials.

Compensation in Clinical Trials

Compensation varies depending on the study, number of visits, time commitment, and participation requirements. Some clinical trials may also reimburse travel-related expenses.

Exact payment details are explained during screening before you decide whether to participate.

For more details, read our guide on how much clinical trials pay in Tampa.

Person discussing clinical trial eligibility with a researcher

Who May Qualify for Paid Clinical Trials?

Eligibility depends on the study. Some clinical trials are designed for individuals with specific medical conditions, while others may enroll healthy volunteers.

Common eligibility factors may include:

  • Age range
  • Medical history or diagnosis
  • Current medications
  • Overall health
  • Ability to attend study visits
  • Study-specific requirements

If you’re unsure whether you may qualify, our team can help review available options with you.

For more detail, read our guide on how to qualify for paid clinical trials.

Santos Research Center clinical research participants

How to Join Paid Clinical Trials in Tampa

Getting started is simple. Our team helps determine whether you may qualify and guides you through each step of the clinical trial process.

  1. Pre-screening

    A quick phone call to review your health history and basic study qualifications.

  2. Informed consent

    You review study details, including your rights, responsibilities, potential risks, and benefits.

  3. Screening visit

    The medical team confirms whether you meet the study requirements.

  4. Enrollment

    If you qualify, you are enrolled and given a study schedule.

  5. Follow-up visits

    The clinical team monitors your health, safety, and response throughout the study.

  6. End of study

    You complete a final visit and return any required study materials.

For more details, read our guide on how to find paid research studies in Tampa.

What Are the Phases of Clinical Trials?

Clinical trials are often conducted in phases to evaluate safety, dosage, effectiveness, and long-term outcomes before a treatment becomes widely available.

Phase I

Focuses on safety and dosage.

Phase II

Studies how well the treatment works and continues safety monitoring.

Phase III

Compares the treatment with standard options in larger groups.

Phase IV

Monitors long-term safety and results after approval.

For more details, read our guide to the phases of clinical trials.

Safety, Consent, and Participant Rights

Clinical trials follow strict safety guidelines designed to protect participants throughout the study process. Before joining a study, participants receive detailed information about the trial, including potential risks, possible benefits, study requirements, and participant rights.

Informed Consent

Before participating, you will review an informed consent document that explains the study in detail so you can make an informed decision about participation.

Voluntary Participation

Joining a clinical trial is always voluntary. You may leave a study at any time without penalty to compensation already earned.

Potential Risks

Like any medical study, clinical trials may involve potential risks, side effects, or additional time commitments. These risks are explained before enrollment.

Placebos in Clinical Trials

Placebos are only used in studies where doing so would not violate medical ethics or withhold appropriate standard care.

Learn more about clinical trial safety in Tampa and what clinical trial studies involve.

Clinical trial participant speaking with a medical research professional

Benefits of Participating in Paid Clinical Trials

Participation in clinical research may provide:

  • Compensation depending on the study
  • No-cost study-related care
  • Access to study-related medical evaluations
  • Close monitoring throughout the study process
  • Access to investigational treatments before wider availability
  • Opportunities to help support future medical research

Some studies may also include lab work, diagnostic testing, physician visits, or additional monitoring related to the research protocol.

Santos Research Center clinical research team

About Santos Research Center

Santos Research Center is a Tampa clinical research facility focused on connecting participants with paid clinical trials and medical studies in Tampa across a wide range of health conditions.

Our team has helped support more than 400 clinical studies involving neurological, infectious disease, metabolic, and chronic health research.

Studies are overseen by experienced physician investigators and supported by trained clinical research coordinators who guide participants throughout the research process.

All studies follow FDA regulations, IRB oversight, and Good Clinical Practice (GCP) guidelines designed to support participant safety and research quality.

Santos Research Center serves participants throughout Tampa Bay, including Town ’n’ Country, Clearwater, Brandon, Riverview, and surrounding communities.

Learn more about Santos Research Center and our clinical research team.

Find Paid Clinical Trials in Tampa

Explore paid clinical trials currently enrolling at Santos Research Center and see whether you may qualify to participate.

  • Compensation may be available depending on the study
  • No-cost study-related care
  • FDA- and IRB-reviewed clinical research
  • Some studies may enroll healthy volunteers

5927 Webb Rd, Tampa, FL 33615

Call (813) 249-9100
See If You Qualify Call (813) 249-9100