Studies
Advancing Medicine Through Innovative Clinical Trials At Pines Care Research Center (PCRC), our unwavering commitment to medical progress fuels every study we conduct. With a focus on precision, full regulatory compliance, and compassionate patient care, we’ve successfully completed over 50 clinical trials across diverse therapeutic areas. Our robust infrastructure and experienced team enable us to manage 10-15 studies annually, ensuring high-quality execution and timely results for sponsors and participants alike.
(Stratified by ICD-10 Diagnostics)
This extensive, stratified patient database — built from
our integrated private practice — allows for
rapid, targeted recruitment, matching participants
to protocols with exceptional efficiency. Sponsors
benefit from diverse, real-world demographics, while
patients gain access to cutting-edge therapies.
Our Therapeutic Areas of Expertise
We specialize in a wide array of therapeutic domains, drawing on our multidisciplinary team’s deep knowledge to deliver reliable outcomes in Phase II–IV trials:
Internal Medicine
Comprehensive care for chronic conditions like hypertension and diabetes.
Endocrinology
Trials focused on hormone disorders, thyroid issues, and metabolic health.
Nephrology
Research into kidney diseases, dialysis innovations, and renal therapies.
Neurology
Studies on neurological disorders, including Alzheimer’s, migraines, and neuropathies.
Psychiatry
Advancing mental health treatments for depression, anxiety, and bipolar disorders.
Pulmonary
Respiratory trials for asthma, COPD, and lung infections.
Gastroenterology
GI research covering IBS, Crohn’s disease, and liver conditions.
Anesthesiology
Pain control and perioperative care innovations.
Urology
Trials in prostate health, urinary tract issues, and bladder disorders.
Ophthalmology
Eye health studies, including glaucoma and retinal diseases.
Dermatology
Skin condition research for acne, psoriasis, and eczema.
Podiatry
Foot and ankle trials, focusing on diabetic foot care and orthotics.
Vaccines
Immunization development for infectious diseases and preventive health.
Men’s Health
Specialized studies in testosterone, prostate, and reproductive issues.
Women’s Health
Research into menopause, fertility, and gynecological conditions.
Pain Management
Chronic pain therapies, including opioids alternatives and neuromodulation.
Infectious Diseases
Trials for HIV, hepatitis, and emerging pathogens.
Volunteer for a Study
Your Opportunity to Make a Difference Interested in contributing to groundbreaking medical advancements?
As a volunteer, you’ll receive expert care, potential access to new treatments, and compensation for your time — all while helping shape the future of healthcare. We provide complimentary transportation to and from our Pembroke Pines facility for added convenience.
Complete the form below to join our patient database. Our team will review your information and contact you about upcoming studies matching your profile and eligibility.
Why Participate in Clinical Trials?
A Guide for Patients and Advocates Clinical trials are the cornerstone of medical innovation, bridging the gap between laboratory discoveries and real-world treatments that save lives and improve quality of life. If you’re a potential participant, family member, or advocate, understanding the process can empower you to get involved confidently.
Benefits for Participants:
- Access to Cutting-Edge Therapies: Gain early exposure to new medications, devices, or procedures not yet available to the public — often at no cost, with all study-related care covered.
- Expert Medical Monitoring: Receive thorough health evaluations from board-certified specialists like Dr. Jaynier Moya, including free screenings, lab tests, and follow-ups that could detect issues early.
- Compensation and Support: Earn stipends for time and travel, plus perks like our complimentary transportation service to ensure participation is accessible and hassle-free.
- Contributing to a Greater Good: Your involvement helps develop treatments for conditions affecting millions, potentially benefiting your community, loved ones, or future generations.
The Process: What to Expect
- Screening and Enrollment: After submitting your form, we’ll conduct a confidential phone or in-person screening to assess eligibility based on age, health history, and study criteria. No obligation — you can withdraw anytime.
- Informed Consent: We’ll explain the study in detail, including potential risks/benefits, using clear language (available in English/Spanish). Sign only if you’re comfortable.
- Study Visits: Attend scheduled appointments at our state-of-the-art facility, where our caring team ensures your comfort. Visits may include exams, medication administration, or questionnaires — all under strict safety protocols.
- Follow-Up and Close-Out: Post-study, we provide ongoing support and share results when available, helping you transition back to standard care.
Safety First:
Your Protection is Paramount All trials at PCRC are approved by Independent Review Boards (IRBs) and adhere to FDA guidelines. We prioritize participant rights through:
- Strict confidentiality via HIPAA compliance.
- Continuous monitoring for side effects, with immediate access to medical intervention.
- Diverse inclusion to ensure trials reflect real populations, promoting equitable healthcare.
Advocating for Participation: As an advocate — whether a healthcare provider, community leader, or loved one — encourage informed involvement by sharing resources like ClinicalTrials.gov or our site. Trials need diverse volunteers to succeed; your voice can demystify the process and inspire others. At PCRC, we’re here to answer questions and provide educational materials.