Massive cancer registry aims to improve Real-World treatment insights
NCT ID NCT06877884
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study is a large registry that collects information from adult cancer patients during their routine care. Researchers will track treatments, side effects, and outcomes to better understand how cancer is managed in real-world settings. Up to 20,000 participants will be enrolled at participating oncology centers. The goal is to generate high-quality data that can help improve future cancer research and care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this registry could help researchers better understand real-world cancer treatments and outcomes, potentially improving future care.
- What could go wrong
- This is an observational study, not a treatment trial. It collects data only and does not test any new therapy, so direct patient benefits are limited.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 20,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2022
- Expected to finish
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Jan 2099
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All patients at oncology sites participating in the registry.
- Ages
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18 to 120 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Be a patient at a site (oncology) participating in the Registry Be at least 18 years old Be able and willing to provide signed informed consent Exclusion Criteria: Prisoners/imprisonment at time of screening for eligibility Patients who cannot consent without utilization of a legally authorized representative
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
7 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
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Contact
Email: •••••@•••••
Locations
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Bayhealth Cancer Center- Sussex
RECRUITINGMilford, Delaware, 19963, United States
Contact Email: •••••@•••••
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Bayhealth Cancer Center-Kent
RECRUITINGDover, Delaware, 19901, United States
Contact Email: •••••@•••••
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Lankenau Medical Center
RECRUITINGPaoli, Pennsylvania, 19301, United States
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New Mexico Oncology Hematology Consultants
RECRUITINGAlbuquerque, New Mexico, 87109, United States
Contact Email: •••••@•••••
Contact Email: •••••@•••••
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Northwest Oncology & Hematology
RECRUITINGElk Grove Village, Illinois, 60007, United States
Contact Email: •••••@•••••
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Oncology Consultants, P.A.
RECRUITINGHouston, Texas, 77030, United States
Contact Email: •••••@•••••
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Pacific Cancer Care
RECRUITINGMonterey, California, 93940, United States
Contact Email: •••••@•••••
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Other studies related to the condition(s) this trial covers.
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