Clinical Research
Orso Health Clinical Research
Advancing Medicine Through Scientific Discovery
Advanced Clinical Research Collaboration and Innovation
Advanced Clinical Research Collaboration and Innovation
At Orso Health, we connect patients, physicians, and research sponsors to groundbreaking studies that drive medical progress. By participating in clinical research, individuals contribute to advancements that improve healthcare for future generations.
Clinical Research at a Glance
- Advances medicine by developing new treatments, medications, and medical devices.
- Provides patient benefits such as access to innovative therapies, expert medical care, and potential compensation.
- Follows a structured process with screening, informed consent, and study protocols.
- Ensures safety and ethics through regulation by IRBs, the FDA, and other governing bodies.
- Offers versatile programs options ranging from short visits to long-term monitoring.
Driving Medical Innovation
What is Clinical Research?
Clinical research is the foundation of modern medicine. It drives the discovery of new treatments, improves patient outcomes, and enhances our understanding of health and disease. At Orso Health, we connect individuals with cutting-edge clinical trials that contribute to the future of healthcare.
The Science Behind Medical Breakthroughs
Why is Clinical Research Important?
Clinical research helps answer critical medical questions:
- Does a new treatment work?
- Is it safe for patients?
- How does it compare to existing treatments?
- What are its potential side effects?
By conducting controlled studies with volunteers, researchers gain valuable insights that lead to life-changing medical innovations.
A Study in Studies
Types of Clinical Research
Clinical trials are studies that test new drugs, devices, or medical procedures on humans. They help determine whether an innovation is safe and effective for widespread use. Common types of clinical trials include:
Drug Trials
Testing new medications or combinations of treatments.
Medical Device Trials
Evaluating the safety and function of new medical technologies.
Therapy Trials
Assessing new surgical techniques, rehabilitation methods, or behavioral therapies.
Preventive Studies
Investigating vaccines, lifestyle interventions, or nutritional strategies to prevent disease.
Seeking Truth
Observational Studies
Unlike clinical trials, observational studies do not involve experimental treatments. Instead, researchers monitor individuals over time to understand disease progression, risk factors, and treatment outcomes.
Examples of observational studies include:
- Studying the long-term effects of a condition.
- Identifying risk factors for chronic diseases.
- Evaluating patient responses to existing treatments.
The Four Phases of Testing
Phases of Drug and Treatment Clinical Trials
Clinical trials follow a step-by-step process to ensure safety and accuracy. Each phase is crucial in determining whether a treatment should be approved for public use.
Phase I
Tests a treatment’s safety and dosage in a small group of healthy volunteers.
Phase II
Evaluates the treatment’s effectiveness and side effects in a larger group of patients.
Phase III
Confirms effectiveness, compares it to existing treatments, and monitors side effects in a broad population.
Phase IV
Conducted after FDA approval to gather long-term safety and effectiveness data.
Patients With Purpose
Who Can Participate in Clinical Research?
Clinical trials need volunteers from all backgrounds to ensure treatments are effective for diverse populations. Each study has specific criteria, including:
- Age, gender, or ethnicity.
- Medical history and current health status.
- Lifestyle factors, such as smoking or diet.
Participation is always voluntary, and safety is a top priority.
Safety First
Ethics & Safety in Clinical Research
Every clinical trial follows strict ethical and regulatory guidelines to protect participants. Studies are overseen by:
Institutional Review Boards (IRBs
Independent committees that ensure participant safety and study integrity.
Regulatory Agencies
Organizations like the FDA (U.S.), EMA (Europe), and WHO (global) enforce strict protocols.
Informed Consent Process
Before joining a study, participants receive detailed information and can ask questions before giving consent.
Participants can withdraw from a study at any time, for any reason.
Clinical Research
Frequently Asked Questions
No, participation in clinical trials is typically free. In many cases, participants receive compensation for their time and travel. The treatments, procedures, and any necessary follow-up are usually covered by the research program.
By participating, you may gain early access to innovative treatments, help advance medical knowledge, and play a vital role in improving healthcare for others. Additionally, some studies provide participants with close medical monitoring throughout the trial.
The duration of a clinical research program varies based on the type of study. Some trials last a few weeks, while others may continue for months or even years. The study team at Orso Health will provide you with a clear timeline before you enroll.
Participants can leave a clinical research program at any time, for any reason. Your decision to withdraw will not impact your future care or your relationship with your healthcare provider. The study team will ask for feedback to understand your experience.
This depends on the type of study. In some trials, participants know the treatment they are receiving, while others are “blinded,” meaning neither the participants nor the researchers know who receives the active treatment or placebo. This helps ensure unbiased results.
Our clinical trials cover a wide range of health topics. Some focus on individuals with specific serious medical conditions, while others explore preventive care, new diagnostic methods, or treatments for milder issues.
