Data combo could forecast pancreatic Cancer's next move

NCT ID NCT07561814

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Recruiting now This study
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
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 Results may not be published yet.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.
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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

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Status unknown
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First seen Jun 27, 2026 · Last updated Jul 02, 2026 · Updated 1 time

Summary

This observational study looks at whether combining CT scans, blood tests, and pathology reports can more accurately predict how pancreatic cancer will progress. Researchers will collect existing medical records from about 1,030 participants who had surgery for pancreatic cancer. Participants will not receive any extra tests or treatments, but will get a follow-up call every 3 months for up to 3 years. The goal is to improve estimates of survival and cancer recurrence risk.

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Study facts

What this study's own registry entry says, in plain language.

Participants

About 1,030 people

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

Started

Dec 2025

Expected to finish

Dec 2029

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

The study population will be drawn from patients receiving surgical treatment for pancreatic cancer at two academic medical centers in China: the Department of Pancreatic Surgery, Zhongshan Hospital, Fudan University (Shanghai) and the Third Xiangya Hospital, Central South University (Changsha). The retrospective cohort includes patients diagnosed between January 2023 and December 2025, identified from hospital electronic health records. The prospective cohort will comprise newly diagnosed patients enrolled consecutively. Both cohorts originate from the same clinical settings, representing a tertiary hospital-based population with consistent diagnostic and treatment standards.

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: * Age ≥ 18 years. * Histologically or cytologically confirmed diagnosis of pancreatic cancer. * Availability of preoperative and postoperative contrast-enhanced CT images at the participating center; patient records include corresponding clinical data, postoperative pathological reports, and preoperative and postoperative blood test results. * Underwent surgical treatment for pancreatic cancer at a participating center of this study. Exclusion Criteria: * Age \< 18 years (minors). * Presence of other severe diseases (e.g., severe liver or kidney failure, cardiovascular or cerebrovascular diseases, malignancies other than pancreatic cancer); pregnant or breastfeeding women; individuals with mental illness; * patients unable to comply with follow-up or provide informed consent. * Presence of significant outliers (e.g., laboratory values exceeding 10 times the normal range without clinically reasonable explanation) or samples with excessive missing data.

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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

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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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  3. A doctor treating you

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Contacts and locations

Locations

  • Zhongshan Hospital Affiliated to Fudan University

    RECRUITING

    Shanghai, Shanghai Municipality, China

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