Santos Research Center · Tampa, Florida

Obesity Clinical Trials in Tampa, FL

Santos Research Center lists currently enrolling obesity clinical trials in Tampa on this page. Each study has its own eligibility requirements, visit schedule, study-related care, and compensation details.

Review the available study information below, then contact our research team to begin the pre-screening process. Applying does not guarantee that you will qualify or be enrolled.

Not sure how screening works? Learn more about qualifying for a clinical trial in Tampa.

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

Obesity clinical trial participant speaking with a research professional

Accepting New Patients

Currently Enrolling Obesity Clinical Trials

Accepting New Patients

Study 1: Current Phase 3 Obesity Study

Santos Research Center invites individuals to participate in a pivotal Phase 3 clinical trial focused on innovative treatment methods for obesity.

This trial is part of a comprehensive research initiative to develop more effective strategies for weight management and overall health improvement.

Study-related phone and in-clinic visits with Physician at no cost

See If You May Qualify

Details

Start Date: March 2024
Phase: Phase 3
Insurance: No insurance is needed
Benefits: Medication for weight loss and compensation up to $2,000

Eligibility

Male or female, age >=18 years
BMI >=27 kg/m2
Medical History of Heart Failure, Myocardial Infarction, or chronic kidney disease (CKD)

Excluding

Previous treatment with glucagon-like peptide-1 receptor (GLP-1R) agonists 3 months before the 1st visit (Semaglutide)
Type 1 Diabetes Mellitus
History of either chronic or acute pancreatitis

What Happens After You Apply?

Applying begins with a simple contact form or phone call. You do not need to send detailed medical information through the website.

Submit Your Information

Complete the contact form or call Santos Research Center at (813) 249-9100. Let the team know that you are interested in an obesity clinical trial listed on this page.
Please do not include detailed diagnoses, medication lists, or other sensitive health information in the website form.
Complete a Private Pre-Screening Call

A research coordinator will contact you and ask a few initial questions about your age, height and weight, medical history, current and previous medications, health conditions, and availability for study visits.
This call helps the research team determine whether the study may be a possible fit.
Attend a Screening Visit

If you appear to meet the initial requirements, you may be invited to Santos Research Center for a screening visit.
The screening process may include health assessments, laboratory testing, medical history review, or other evaluations required by the study protocol.
Review the Study Before Deciding

Before you agree to participate, the research team will explain the study purpose, visits, duration, possible risks and benefits, compensation requirements, and your rights as a participant.
You will have time to ask questions before deciding whether to join.

Why Participate in an Obesity Clinical Trial?

Obesity clinical trials help researchers study potential new approaches to weight management and related health concerns.

By participating, you may have the opportunity to:

Receive study-related visits and evaluations at no cost
Receive possible compensation for time and travel
Be monitored by an experienced clinical research team
Contribute to research that may improve future obesity care
Help researchers better understand weight management and related health conditions

Participation may or may not provide a direct medical benefit. The research team will explain the possible risks and benefits during the informed consent process.

Study-Related Care and Compensation

Study-related care and compensation vary by clinical trial. Depending on the study, participants may receive study-related visits, exams, testing, or investigational treatment at no cost.

Some studies may also offer compensation for time, travel, or study-related activities. The amount, payment schedule, and requirements depend on the individual research protocol.

The research team will explain all study-related costs, compensation, visit requirements, and other details during screening and informed consent before you decide whether to participate.

Learn more about how clinical trial compensation works in Tampa.

Your Safety and Rights as a Participant

Clinical trials follow a research plan called a protocol. The protocol explains who may participate, what procedures will take place, and how participant safety will be monitored.

Before any study procedures begin, you will review an informed consent form with the research team. This process gives you information about the study and allows you to ask questions.

Participation is voluntary. You can decide not to join, and you may choose to leave the study after enrolling. The research team will explain any recommended safety follow-up if you decide to withdraw.

How clinical trials protect participant safety Informed consent in clinical trials

What to Expect During Participation

Every clinical trial is different. Your visit schedule and study procedures will depend on the research protocol.

Participation may include:

Scheduled phone calls
Visits to the Tampa research center
Physical exams
Laboratory tests
Study medication, treatment, or other research procedures
Questions about your health
Ongoing safety monitoring
A final study visit

The research team will explain how many visits are required and what will happen at each visit before you enroll.

You should continue to receive routine medical care from your regular healthcare providers. Participation in a clinical trial does not replace your usual medical care.

Why Choose Santos Research Center?

Santos Research Center has conducted more than 400 clinical trials and continues to support medical studies in Tampa across multiple therapeutic areas.

Participants choose our Tampa clinical research facility because we offer:

Experienced research professionals
FDA-regulated clinical studies
IRB-approved research protocols
English- and Spanish-speaking staff
No-cost study-related care
No insurance requirement for qualifying studies
A convenient Tampa location
Clear communication throughout the research process

Our team works with participants, physician investigators, study sponsors, and clinical research organizations to help advance medical research throughout the Tampa Bay area. Learn more about Santos Research Center.

What Participants Say

Participants value the attentive staff, clear communication, and welcoming environment at Santos Research Center.

I recently had the pleasure of participating in a trial at Santos Research Center. The attentive staff took care of my every need, and Dr. Gonzalez was incredibly professional.

Suzanne Franco Google Review. Edited for clarity.

Very professional, always attentive and willing to answer any questions. The best I’ve met in Tampa Bay so far.

Sadi Martin Google Review. Translated from Spanish by Google.

Excellent service from the doctors and staff, always willing to answer any questions. Everything was very clean and welcoming. I highly recommend them!

Juana Elena Romero Fernandez Google Review. Translated from Spanish by Google.

FAQ

Frequently Asked Questions About Obesity Clinical Trials

Clinical trial participant speaking with a Santos Research Center professional

How do I know if I qualify for the obesity clinical trial?

Review the eligibility and exclusion criteria listed on this page. A research coordinator will also review your health history, BMI, medications, and other study requirements during pre-screening. Final eligibility is determined after all required screening steps are completed.

Do I need health insurance?

No. The current study details state that health insurance is not required. Study-related visits and procedures are provided at no cost.

How much does the obesity clinical trial pay?

The current study details state that qualified participants may receive compensation up to $2,000. The exact payment schedule and requirements will be explained during screening. Compensation may depend on completed visits and study activities.

Does submitting the contact form mean I am enrolled?

No. Submitting the form only tells Santos Research Center that you are interested. A research coordinator will contact you to complete an initial pre-screening. Further evaluation is required before enrollment can be confirmed.

What happens during the pre-screening call?

A coordinator may ask about your age, height, weight, medical history, medications, and current health conditions. The purpose is to determine whether it makes sense to schedule a screening visit.

Will I have to stop taking my current medications?

Do not stop or change any medication unless instructed by a qualified healthcare provider. The research team will review your medications during screening and explain whether any medication affects your eligibility.

Can I leave the study after I enroll?

Yes. Participation in clinical research is voluntary. You may choose to leave the study at any time. The research team may recommend follow-up steps to protect your safety.

What if I do not qualify?

Not qualifying for one study does not mean you cannot participate in another study. You can review currently enrolling clinical trials in Tampa or ask the research team whether another opportunity may be available.

Other Clinical Trials in Tampa

Santos Research Center conducts clinical research across several health conditions.

See If You May Qualify for an Obesity Clinical Trial

If you are interested in the currently enrolling obesity study, contact Santos Research Center to begin the pre-screening process.

A research coordinator will review the study requirements, answer your questions, and explain what happens next.