Simple blood test aims to spot multiple cancers early
NCT ID NCT05181826
First seen Jul 10, 2026 · Last updated Jul 10, 2026
Summary
This study collects blood samples from healthy people, those with benign diseases, and cancer patients to develop a multi-analyte blood test. The test looks for DNA methylation markers that may indicate the presence of various cancers, especially liver cancer. Researchers aim to measure how sensitive and specific the test is, and to identify conditions that could cause false results.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multi-analyte Blood Test
- What this could lead to
- If successful, this blood test could help detect multiple cancers early, potentially improving treatment outcomes and survival rates.
- What could go wrong
- This is an observational study focused on test development, not a treatment. The test may not prove accurate enough for widespread use, and false positives or negatives are possible.
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 1,200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2019
- Expected to finish
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Jan 2028
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
Healthy subjects, subjects diagnosed with active cancer, subjects in cancer remission, and subjects diagnosed with a benign disease will eligible to participate in this study.
- Ages
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18 years and older
- Sex
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Anyone
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: 2.1.1 Age 18 years or older. 2.1.2 A diagnosis of cancer, cancer remission, benign disease (benign tumor, diabetes, liver cirrhosis, chronic hepatitis B or hepatitis C virus infection, Chronic obstructive pulmonary disease, etc.) or apparently healthy volunteers. . Exclusion Criteria: 2.2.1 Patients that are unwilling or unable to sign the Informed Consent Form will be excluded. 2.2.2 Approximately 50 mL of blood will be drawn from participants within an 8-week period under this protocol. Patients that have already given 50 mL of blood within this time frame will be excluded.
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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 places running it
6 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
Locations
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Allina Health, Virginia Piper Cancer Institute
RECRUITINGCoon Rapids, Minnesota, 55433, United States
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Liver Center of Texas
RECRUITINGDallas, Texas, 75234, United States
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Methodist Hospital
RECRUITINGRichardson, Texas, 75082, United States
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Methodist LeBonheur Healthcare
RECRUITINGMemphis, Tennessee, 38104, United States
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Torrance Memorial Physician Network - Cancer Care
ACTIVE_NOT_RECRUITINGRedondo Beach, California, 90277, United States
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VPCI Oncology Research
RECRUITINGMinneapolis, Minnesota, 55407, United States
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Virginia Piper Cancer Institute Mercy Hospital-Unity Campus
RECRUITINGFridley, Minnesota, 55432, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Évaluation de la détresse post-traumatique relative au cancer dans l'année suivant le diagnostic chez les patients et les aidants et identification de leurs attentes envers un accompagnement personnalisé
- Development and pilot implementation of a novel remote patient monitoring program for cancer patients initiating cancer-directed therapy: the SHIELD (Smart health integration for early life-saving detection)
- The feasibility of electrical impedance tomography to guide non-invasive respiratory interventions in chronic respiratory disease
- The promoting resilience in stress Management-Social needs (PRISM-SN) intervention for adolescents and young adults with cancer: a randomized controlled trial
- An equity focused intervention to improve utilization of guideline concordant extended venous thromboembolism prophylaxis after major cancer surgery
- The effect of gamified sleep hygiene education on sleep quality and fatigue levels in chemotherapy patients