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Can blood tests predict liver Cancer's return?

NCT ID NCT06141564

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study is collecting blood and tissue samples from 360 people with early-stage liver cancer who have had surgery to remove their tumors. Researchers want to find biological markers that could predict if the cancer will come back. The goal is to better understand the immune system's role in recurrence and eventually improve treatment strategies.

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 could help doctors predict which patients are at high risk of liver cancer returning after surgery, and guide more personalized immunotherapy.
What could go wrong
This is an observational study, not a treatment trial. It may not lead directly to new therapies, and the findings might not apply to all liver cancer patients.

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

About 360 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2023

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Early stage HCCs who are eligible for hepatectomy Cirrhosis due to any etiologies, MELD \<= 15 Chronic hepatitis due to any etiologies, without cirrhosis or HCC

Ages

18 years and older

Sex

Anyone

Show 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: * Provision of signed and dated informed consent form * Collection of biosamples at baseline (sera, liver cancer and non liver cancer tissues, Peripheral blood mononuclear cells (PBMCs)) each of the 3-month interval follow ups (serum and PBMCs) for a total of 4 during the study follow up duration 1 year post-hepatectomy. * Early-stage HCC eligible for hepatectomy for curative intention. Early HCC (Stage A) is limited to a single tumor \<5 cm in diameter or three tumors that are each \<3cm. * Stated willingness to comply with all study procedures and availability for the duration of the study and up to 3 years post-study follow up * Adults aged 18 or older * Both genders and all ethnicities * Willingness to give written, informed consent to be enrolled into the study database * Reside in Vietnam at the time of study and provides contact information (email and/or cell phone number for texting) * No prior or current treatment of HCC * No cancer history within 5 years * No participation in other trial for HCC Treatment * No significant hepatic decompensation * No hepatorenal syndrome * Alpha fetoprotein (AFP) test labs within 90 days irrespective of AFP titer * Two phone numbers and personal identification numbers (CMND number) * No known AIDS related diseases * No significant co-morbid conditions with life expectancy \<2 years Exclusion Criteria: * Individuals who cannot, do not want to, or refused to sign the informed consent form (ICF) * Any serious or active medical or psychiatric illness, which, in the opinion of the investigator, would interfere with patient treatment, assessment or compliance with the protocol * Documentation was not adequate * Known HIV positive * Taking immunosuppressants * Having any autoimmune diseases based on clinical and/or laboratory availabilities

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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.

Contacts and locations

Locations

  • 108 Military Central Hospital

    Hanoi, Vietnam

More trials for these conditions

Other studies related to the condition(s) this trial covers.