IRB-reviewed studies
Every study at VMRC runs under Institutional Review Board oversight and informed consent.
Patient Recruitment
Explore available studies in Miami and learn how to take part.
Your information is protected and confidential.
Current studies
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Track record
Pharmaceutical sponsors, biotech companies and academic research networks have run their protocols here — from Phase I to Phase III, in adults, adolescents and young children. Each registered study links to its public record.
30 studies shown
Chronic idiopathic constipation
Asthma
Severe alopecia areata, adolescents
IBS with constipation, ages 6–11
Long COVID rehabilitation
COPD
IBS with constipation, pediatric long-term safety
Functional constipation in infants
Eosinophilic asthma
Severe eosinophilic asthma
Interstitial cystitis / bladder pain syndrome
Strep A rapid diagnostic test
Prevention of symptomatic COVID-19
Long COVID
Lung cancer screening
COPD with exacerbations
COVID-19 in high-risk outpatients
Uncomplicated urinary tract infection
Functional constipation, ages 2–5
IBS with constipation, adolescents
Irritable bowel syndrome with diarrhea, pediatric long-term
Active ulcerative colitis
Moderate to severe Crohn's disease
Functional constipation and IBS-C, pediatric
Functional constipation and IBS-C, pediatric long-term safety
Oral lichen planus
Uncomplicated urinary tract infection
Moderate to severe ulcerative colitis
Moderate to severe Crohn's disease
Irritable bowel syndrome with diarrhea, pediatric
Phase, ages and start year come from each study's public record on ClinicalTrials.gov. Status refers to VMRC's participation as a site.

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How participation works

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Before you decide
A research study that evaluates a treatment under a written protocol. Every protocol is reviewed and approved by an independent ethics board (IRB) before a single participant is enrolled, and the study team follows it visit by visit.
Study visits and study procedures are provided at no cost to you, and no insurance is required to participate. What each study covers, including the investigational medication, is written in its consent form, which you review before agreeing to anything.
A licensed physician serves as principal investigator and is responsible for your care throughout the study. An independent IRB reviews the protocol before it starts and continues to oversee it, and every visit is documented under the supervision of the study's principal investigator.
Studies that offer compensation pay for your time and travel, not for taking a medication. The exact amount and schedule are written in the consent form for that specific study, and you review it before agreeing to anything.
Yes, at any time and for any reason. Participation is voluntary from the first visit to the last; withdrawing does not affect your regular medical care and you do not have to explain your decision.
Your records are kept confidential under Florida law and the study's consent form. Data shared with a study sponsor is coded, and your name is not used in any published result.
Still deciding?Talk it through with our team
Why people trust us
Every study at VMRC runs under Institutional Review Board oversight and informed consent.
Your information is protected, confidential, and handled under our Notice of Privacy Practices.
English or Spanish, from the first call to your last visit — with a team that knows you by name.
Not sure where to start
Our AI study assistant can guide you in English or Spanish.