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Clinical Trial Finder

Finding the Right Trial Shouldn’t Be the Hardest Part of Getting Well

Living with a chronic or serious illness means constantly looking for what’s next — a better treatment, a new option, a reason for hope. Clinical trials are often that next step, offering access to emerging therapies before they’re widely available. Yet for most patients, finding and understanding those options is harder than it should be.

This tool is here to make it simpler. Search below to find actively recruiting clinical trials matched to your condition, with results pulled directly from ClinicalTrials.gov — the official registry maintained by the U.S. National Library of Medicine. Every result you see is a real study, currently open, and looking for participants.

At Accessia Health, we believe access to better care shouldn’t depend on how well you can navigate a system. This is one small way we’re working to change that.

Clinical Trial Search

This clinical trial finder is provided by Accessia Health as an informational resource to help patients explore potential treatment options. It does not constitute medical advice.  Trial data is sourced directly from ClinicalTrials.gov, a database maintained by the U.S. National Library of Medicine (NLM). Accessia Health does not create, verify, or endorse any individual trial listing. Eligibility, availability, and enrollment status may change — always confirm details directly with the trial sponsor or your healthcare provider.

By using this tool, you acknowledge that Accessia Health is not responsible for decisions made based on this information. For personalized guidance, speak with your physician or specialist.

How do I use this tool?

  1. Type your condition into the search bar and click Find Trials.
  2. The table will display all currently recruiting clinical trials matching your condition, pulled in real time from ClinicalTrials.gov.
  3. Each row shows the trial name, its status, phase, and the conditions being studied.
  4. Click “View Trial” to see the full listing including location, contact information, and detailed eligibility criteria.

Results originate from ClinicalTrials.gov. Listing a study here does not imply that Accessia Health recommends it. Talk to your doctor before joining a trial.

Did you know?

500,000

clinical studies are registered on ClinicalTrials.gov across all 50 states and 222 countries

28%

of patients avoid Phase I trials due to fear their insurance won't cover participation costs

FAQs

  • Clinical Trials

    • Clicking “View Trial” on any result will take you to the full listing on ClinicalTrials.gov, where you’ll find the trial’s contact information and the name of the site coordinator. The enrollment process varies by trial but typically starts with a screening call or visit to confirm eligibility. Learn more about the enrollment process on ClinicalTrials.gov →

    • Compensation varies by trial. Some studies offer payment for time and travel; others do not. This information is typically disclosed in the full trial listing. Financial barriers to participation — such as travel costs or lost wages — are something Accessia Health may be able to help with. Learn more about trial participation costs →

    • Clinical trials in the U.S. are regulated by the Food and Drug Administration (FDA) and must be registered on ClinicalTrials.gov under the FDA Amendments Act. Each trial must also be reviewed and approved by an independent Institutional Review Board (IRB) to protect participant safety. Learn more about how trials are regulated →

    • No. Accessia Health does not sponsor or operate any of the trials listed here. This tool pulls live data directly from ClinicalTrials.gov, the official registry maintained by the U.S. National Library of Medicine. Our role is patient navigation — helping you understand your options and remove the financial and logistical barriers that can stand between you and enrollment.

    • Informed consent is the process by which a researcher explains all aspects of a trial to you before you decide whether to participate. It covers the trial’s purpose, duration, procedures, risks, benefits, and your rights as a participant. Signing an informed consent form is not a contract — you can still withdraw from the trial at any time. Learn more about informed consent →

    • All trials registered on ClinicalTrials.gov are required to follow strict ethical and regulatory guidelines, including review by an Institutional Review Board (IRB) before they can begin enrolling participants. You have the right to withdraw at any time without penalty. Learn more about participant protections →

    • Every trial has eligibility criteria — a set of requirements a person must meet to participate. These include inclusion criteria (characteristics you must have) and exclusion criteria (characteristics that would prevent participation).

    • A clinical trial is a research study involving human volunteers intended to add to medical knowledge. Trials test new drugs, medical devices, procedures, or behavioral interventions to evaluate their safety and effectiveness. There are two main types: interventional studies (which test a treatment) and observational studies (which collect data without intervening).

    • Every result in this table shows “Recruiting,” meaning the trial is actively enrolling participants right now. This tool is pre-filtered to show only recruiting studies — completed, terminated, or not-yet-open trials are excluded from your results. To find additional trials, which are not recruiting or have a different status, visit https://clinicaltrials.gov/

    • Clinical trials run in phases, each designed to answer a specific question about a treatment:

      • Phase I — Is it safe? Tests in a small group to evaluate dosage and side effects.
      • Phase II — Does it work? Gathers early data on effectiveness while continuing safety evaluation.
      • Phase III — Is it better? Compares the treatment against the current standard of care in a larger population. FDA approval is typically based on Phase III results.
      • Phase IV — What happens long term? Studies conducted after FDA approval to monitor real-world safety and effectiveness.

      Some trials — particularly those studying devices or behavioral interventions — may show “N/A” for phase.