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Ulcerative Colitis (Disorder)NCT07721987

Development and External Validation of a Machine Learning Model for Pre-Endoscopic Prediction of Montreal Disease Extent (E1/E2/E3) in Ulcerative Colitis Using Symptoms, Signs, and Laboratory Tests: A Multicenter Retrospective Observational Study

An observational study of Ulcerative Colitis (Disorder), run by Beijing University of Chinese Medicine.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This multicenter retrospective observational study aims to develop and externally validate a machine learning model that predicts Montreal ulcerative colitis (UC) disease extent (E1: limited/proctitis; E2: left-sided; E3: extensive) using pre-endoscopic clinical information, including symptoms, signs, and laboratory… Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Ulcerative Colitis (Disorder)
How many people
1,500 participants
Where
No sites listed yet
Study dates
20 Nov 2015to 1 Sep 2026
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 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adults with UC from four hospitals in China (2020-2025). Development cohort: Centers A (Dongfang Hospital, BUCM) and B (Dongzhimen Hospital, BUCM). External validation cohort: Centers C (BUCM Third Affiliated Hospital) and D (Yantai Hospital of Traditional Chinese Medicine).

Who may be able to join

  • Confirmed diagnosis of ulcerative colitis by endoscopy ± histopathology.
  • Montreal disease extent classifiable as E1 (limited), E2 (intermediate/left-sided), or E3 (extensive) and mapped to study labels 1/2/3.
  • Pre-endoscopic baseline data available: demographics, symptoms, signs, and laboratory tests used as model predictors.
  • Predictors collected before or independent of endoscopic findings used for the outcome label (endoscopic extent not used as input).
  • One index visit per patient (duplicate/non-index visits excluded).

Who cannot join

  • Non-UC diagnosis or Montreal extent not assignable.
  • Missing patient identifier/linkage or unlabelable outcome.
  • Incomplete endoscopic gold standard for Montreal extent classification.
  • Duplicate or non-index visits.
  • Critical predictor data unavailable and not handled by the prespecified modeling pipeline

About this study

Official title: Development and External Validation of a Machine Learning Model for Pre-Endoscopic Prediction of Montreal Disease Extent (E1/E2/E3) in Ulcerative Colitis

This multicenter retrospective observational study aims to develop and externally validate a machine learning model that predicts Montreal ulcerative colitis (UC) disease extent (E1: limited/proctitis; E2: left-sided; E3: extensive) using pre-endoscopic clinical information, including symptoms, signs, and laboratory tests. The model is intended to assist clinical assessment before endoscopic confirmation and is not designed to replace colonoscopy or histopathology. Data from development centers (Centers A and B) will be used for model development with nested cross-validation; data from independent external centers (Centers C and D) will be used for external validation only.

Medical subject headings
Colitis, Ulcerative

What is being measured

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

  1. Macro one-vs-rest area under the receiver operating characteristic curve (macro AUC-OVR) for three-class Montreal extent prediction (E1 vs E2 vs E3) in the external validation cohort (n=247).

    Measured: At index visit / endoscopic assessment

Timeline

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

  1. First posted23 Jul 2026
  2. Study start20 Nov 2015
  3. Primary completion1 Aug 2026
  4. Study completion1 Sep 2026 (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
Other
Time perspective
Retrospective
Enrolment
1,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07721987
Sponsor's protocol ID
2026BZYLL0603
Status last verified
Aug 2026
First submitted
19 Jul 2026
Last updated
18 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Due to the restrictions of the informed consent form approved by the Institutional Review Board (IRB), patients were only consented for the use of their data in this specific clinical prediction model study. Broad data sharing was not covered in the original ethical approval, and obtaining re-consent from all 247 participants is not feasible.

Questions about this trial

What is this clinical trial studying?

An observational study of Ulcerative Colitis (Disorder), run by Beijing University of Chinese Medicine.

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 5 inclusion and 5 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: under way, not looking for participants, as of the sponsor's last update on 18 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Macro one-vs-rest area under the receiver operating characteristic curve (macro AUC-OVR) for three-class Montreal extent prediction (E1 vs E2 vs E3) in the external validation cohort (n=247). (time frame: At index visit / endoscopic assessment). 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 18 Aug 2026.

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