Clinical Trials
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Clinical Trials and Research Studies
With approximately 2,500 active research studies spanning various clinical areas, BIDMC researchers are at the forefront of clinical and translational research, leading advancements in healthcare, treatments and understanding of human physiology and psychology.
Clinical trial participants play a pivotal role in this journey of discovery. Individuals take part in clinical research for many reasons, ranging from altruism to accessing innovative investigational therapies. Whether exploring new treatments, preventive measures, diagnostic methods or quality-of-life enhancements, clinical trials pave the way for improved healthcare outcomes.
For Patients: Finding and Participating in Clinical Trials
To engage in clinical research, you can explore ongoing studies in the Clinical Trial Directory or join the Clinical Research Volunteer Registry, which welcomes participants regardless of medical history. National resources like ResearchMatch also offer opportunities to connect with studies.
Considering participation in clinical trials or research studies presents an opportunity to contribute to medical innovation. Each day, new medical techniques, drug discoveries and device innovations emerge through clinical research, potentially enhancing quality of life.
Clinical research encompasses various types:
- Clinical Trials: Evaluate safety and effectiveness of interventions or therapies
- Observational Studies: Investigate natural relationships in human health without interventions
- Epidemiological Studies: Explore patterns, causes and effects of health and disease across different populations
- Behavioral Studies: Examine how human behavior influences health outcomes
For Researchers: Clinical Research at BIDMC
BIDMC hosts a dynamic and large-scale clinical research enterprise, with thousands of active studies supported by a comprehensive infrastructure. Learn more about clinical research resources available at BIDMC.
More About Clinical Trials
Benefits
- Early access to novel treatments before they become widely available
- Comprehensive medical attention and possibly no cost for additional tests and examinations
- Contribution to advancing medical science
Disadvantages
- Time commitment due to additional visits and tests
- Potential discomfort from discontinuing current treatments
- Uncertainty about the effectiveness of new treatments
Risks
- Possible side effects unique to experimental treatments
- Unknown risks associated with new therapies
Informed consent is a crucial part of clinical research. Through informed consent, participants are empowered to make informed decisions, ensuring their involvement aligns with personal goals and health needs.
- Ensures participants understand study details, potential risks and benefits
- Participation is voluntary, and individuals can withdraw at any time
- Continual updates on treatment information are provided throughout the study
