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Pancreatic CancerNCT07561814

A Study on a Predictive Model for Efficacy and Prognosis of Pancreatic Carcinoma Based on Multimodal Data

An observational study of Pancreatic Cancer, run by Shanghai Zhongshan Hospital at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this observational study is to learn if combining information from CT scans, blood tests, and pathology reports can better predict how pancreatic cancer will progress. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pancreatic Cancer
How many people
1,030 participants
Where
1 siteChina
Study dates
9 Dec 2025to 31 Dec 2029
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: 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.

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site, 1 recruiting
  • Zhongshan Hospital Affiliated to Fudan University

    Shanghai, Shanghai Municipality

    Dongjie Chen, 18221994497, chen_dj@outlook.com

    Recruiting

Other trials in China

About this study

The goal of this observational study is to learn if combining information from CT scans, blood tests, and pathology reports can better predict how pancreatic cancer will progress.

The main questions it aims to answer are:

  • Can combining these types of data more accurately estimate how long a person might survive?
  • Can it better predict the risk of recurrence?

Participants will not have any extra tests or treatments. They will:

  • Allow researchers to collect information from their existing medical records (such as surgery reports, imaging, and lab results)
  • Receive a follow-up phone call for up to 3 years to share health updates(about every 3 months for the prospective cohort).
Keywords
Pancreatic cancer, Multimodal data, Deep learning, Predictive model, Prognosis, CT imaging
Medical subject headings
Pancreatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07561814
Study groupRoleWhat they receive
Retrospective cohortNot described
prospective cohortNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. overall survival

    Measured: 3 years

  2. recurrence free survival

    Measured: 3 years

  3. recurrence status within one year after surgery

    Measured: 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 May 2026
  2. Study start9 Dec 2025
  3. Primary completion31 Jul 2029 (estimated)
  4. Study completion31 Dec 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
1,030 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07561814
Sponsor's protocol ID
B2026-107(2)R
Status last verified
Apr 2026
First submitted
25 Apr 2026
Last updated
2 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Pancreatic Cancer, run by Shanghai Zhongshan Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 2 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

overall survival (time frame: 3 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jul 2026.

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