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Clinical Trials, Made Accessible

For Patients

Explore new treatment options, receive dedicated care, and make informed decisions about your health with support at every step.

Browse Current Studies
The Basics

What is a clinical trial?

A clinical trial is a research study that helps evaluate new medications, treatments, or approaches to care. Trials are carefully designed and monitored to determine whether a treatment is safe and effective before it becomes widely available and participation is always voluntary.

Carefully monitored for safety

Carefully monitored for safety

Carefully monitored for safety

When options feel limited, many patients don’t know where to turn.

If you are managing a chronic or complex condition, you may have experienced:

  • Limited treatment options
  • Short, time-constrained appointments
  • Uncertainty about what to try next

Clinical trials are often not presented as an option — even when they could help.

Clinical Trials

Explore active trials available near you — no referral needed.

Browse Current Clinical Trials

Updated regularly - Across all Orso Health sites

Clinical trials offer another path forward.

Participating in a clinical trial may provide access to:
  • New and emerging treatments
  • Therapies not yet widely available
  • Care from specialized research teams

In many cases, patients receive more frequent monitoring and attention than in standard care.

You are in control.

We understand that joining a clinical trial is a significant decision. Our role is to make the process clear, transparent, and supportive — at every step.

At ORSO Health:

  • Participation is always voluntary
  • You receive clear, complete information before deciding
  • Your safety is our main priority and will be continuously monitored
  • You have a dedicated research coordinator available to answer your questions throughout
  • Study-related visits and travel expenses are covered by the study sponsor — no financial burden to participate
  • Your research care team and physicians will closely monitor your health, safety, and response to treatment throughout your participation

You are never expected to move forward without fully understanding your options.

Most clinical trials take place at large academic centers, often far from where patients live.

ORSO Health changes that by:

  • Embedding trials within local clinics
  • Partnering with physicians in your community
  • Making participation more accessible and convenient

YOUR PATH FORWARD

When taking part in a clinical trial looks like

Five simple steps, all at a clinic near you - ask questions anytime, and you're free to stop whenever you choose.

1

Learn About a Study

Speak with your healthcare provider or research team to determine if a clinical trial may be a good fit for your medical condition and health goals.

2

Complete a Pre-Screening

Answer a few questions about your medical history, current health, and medications to see if you may qualify.

3

Attend a Screening Visit & Provide Informed Consent

Speak with your healthcare provider or research team to determine if a clinical trial may be a good fit for your medical condition and health goals.

4

Participate in the Study

If eligible, you'll receive the study treatment or intervention and attend scheduled visits where the research team monitors your health, collects study data, and supports you throughout.

5

Complete the Study & Follow-Up

Finish your final study visit and any required follow-up appointments. Your participation helps advance medical research and may improve treatment options for future patients.

Why Consider Joining a Clinical Trial?

Clinical trials offer patients access to advanced care, new treatments, and the chance to make a real difference in the future of medicine. Here’s what you can expect:

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

FAQs

About Clinical Trials

A clinical trial is a research study that helps evaluate new medications, treatments, medical devices, or approaches to care. Clinical trials are designed to determine whether a treatment is safe and effective before it becomes widely available.

People participate for many reasons, including access to potential new treatments, receiving additional medical monitoring, helping advance medicine, and contributing to future patient care for their condition or community.

Patient safety is the top priority in clinical research. Clinical trials follow strict regulations and are reviewed by ethics committees called Institutional Review Boards (IRBs). Participants are closely monitored by healthcare professionals throughout the study.

Yes. Participants are monitored by qualified healthcare providers and research staff during the trial. Study related visits, assessments, and follow-up care are outlined in the informed consent form before participation begins.

Many clinical trials provide study-related medications, procedures, and visits at no cost to participants. Some studies may also reimburse for travel or time. The research team will explain any costs or compensation before enrollment.

Yes. Participation is completely voluntary. You may choose to leave a clinical trial at any time and for any reason without affecting your regular medical care.

Informed consent is the process where the research team explains the purpose of the study, procedures, potential risks, possible benefits, and participant rights. You will have the opportunity to ask questions before deciding whether to participate.

Empowering every individual with clear, accessible, and unbiased information so they can actively participate in decisions about their health and treatment options. Learn more about how we serve our patients.

The length of participation varies depending on the study. Some trials last a few weeks, while others may continue for several months or longer. The schedule of visits and expectations will be reviewed with you before participation.

Each clinical trial has specific eligibility criteria based on factors such as age, medical history, current medications, and diagnosis. The research team will conduct a screening process to determine whether the study may be a good fit for you.

You deserve more options — and more support.

We believe access to innovative care and clinical research opportunities shouldn’t depend on where you live or who you know.

We’re here to help you explore what’s possible.

Contact Our Team