Powering the Future of Care
Clinical research helps us better understand health and treatment. Our platform makes it easy to find active studies that may be right for you or your family. We share study information so you can learn about research opportunities and decide whether participation feels right for you.
Who We Are
Led by licensed physicians and experienced research professionals, we connect individuals with clinical trials that are conducted under strict safety and ethical standards. Our goal is to make it easier for patients to learn about research opportunities that help advance medical understanding and future care.
Why Choose Us
Trial Services
We specialize in clinical research studies for respiratory conditions such as asthma, bronchiectasis, COPD, and smoking-related lung changes, as well as podiatry studies focused on diabetes-related foot health and plantar fibromatosis. All studies are physician-led and conducted under strict ethical and safety guidelines to support responsible research and advance medical understanding.
Clinical studies for asthma, bronchiectasis, and COPD evaluating potential new options to support respiratory health.
Clinical trials for diabetic foot ulcers and plantar fibromatosis evaluating potential new approaches to support foot health and mobility.
Clinical studies evaluating traditional cigarettes and e-cigarettes to explore potential differences in exposure and health impact.
Every study involves careful screening, monitoring, and physician oversight to promote safety and high-quality research.
Participation Process
Our participation process is designed to prioritize ethical and regulatory standards, participant comfort, and clear communication throughout each stage of a study. From screening and enrollment to medical evaluations and follow-up, every step is guided by licensed professionals and conducted according to established research requirements. These studies aim to contribute to medical knowledge and support the future of healthcare.
Participants complete a medical evaluation to confirm eligibility for the appropriate study.
Approved participants receive full study details, schedules, and expectations before starting.
During the trial, medical professionals monitor progress, treatment response, and safety.
After completion, participants receive follow-up care and updates on study outcomes when available.
Get Connected
Contact our research team to learn more about current studies and eligibility criteria. We’re here to provide clear information and help you explore available clinical research options so you can decide whether participation may be right for you.
Contact Our Team
FAQ
Find answers about clinical trials, participation, safety, and eligibility from medical professionals to help you understand the process, requirements, and benefits of joining a study safely and confidently.
01 Will a clinical trial affect my regular medical care, and will it cost anything?
You can still see your regular doctor while you are in a clinical trial. With your permission, the study team may share information with your doctor so your care stays on track. Being in the study should not interfere with any important medical treatment you need.
The informed consent form will explain:
If you have questions, ask the study team or your regular doctor before deciding to join.
02 Why do people join clinical trials?
People join for a variety of reasons, including:
Access to new or investigational treatments
Each person’s motivation is unique, and all reasons are valid.
03 How do I know if I qualify for a clinical trial?
Each study has eligibility criteria that include things like age, medical history, diagnosis, medication use, or previous treatments.
These criteria ensure:
A study team member will review your eligibility in detail during screening.
04 Will I know which treatment I receive?
It depends on the study design:
All of this is explained during informed consent.
05 Can I leave a clinical trial after joining?
Yes. Participation is voluntary. You may withdraw at any time for any reason, and your medical care will not be affected.
06 What is informed consent?
Informed consent is the process of providing participants with clear, understandable information about the trial so they can make a voluntary decision about participation. This includes:
07 Will participating affect my regular medical care?
Your regular healthcare providers can continue to treat you. Most trials:
Talk with your doctor about how the trial fits into your overall care.
08What kind of monitoring will I receive?
You will be monitored by licensed medical professionals through regular exams, lab tests, and follow-up visits. Some studies may also include phone check-ins or wearable devices to track your progress, and you can view process to get a clear look at how your monitoring and care are managed throughout the study.
09Will I be paid for participating?
Some clinical trials provide payment or reimburse travel and related expenses as compensation for your time and commitment. Others do not offer payment but cover all study-related medical care and tests at no cost. Compensation details vary by study, so review the participant information carefully or see eligible benefits to learn what applies to you.
10What happens when the study ends?
Once the study concludes:
Ready to Learn More?
Participation in clinical research contributes to a better understanding of health and disease. By joining a study, you may help inform future treatment approaches while receiving study-related evaluations and monitoring as outlined in the research protocol.
