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RecruitingNCT06452550Updated Jun 11, 2024

Neurophenotype Predicts CD Disease Progression

An observational study in Radiomics and Multi-omics, sponsored by First Affiliated Hospital, Sun Yat-Sen University. Recruiting at 1 site in China. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-11.

Sponsored by First Affiliated Hospital, Sun Yat-Sen University · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 4 months ago, but the record still lists the study as recruiting.
  • Started May 2021; still recruiting 5 years 5 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
500
Ages
18 Years to 45 Years
Sex
All
01

Study summary

The goal of this observational study is aimed to develop a novel multimodal neuroimaging-based model to characterize the neurophenotype of Crohn's Disease patients and assess its ability for predicting disease progression, using multiomics data to interpret the model.

Participants will be followed-up of at least six months for patients without disease progression to assess the relationship between neurophenotype and intestinal outcomes.

Read the detailed description

Brain-gut axis plays a crucial role in the pathogenesis of Crohn's disease (CD); however, CD neurophenotype and its impact on intestinal disease progression remain unclear. We aimed to develop a novel multimodal neuroimaging-based model to characterize the neurophenotype of CD patients and assess its ability for predicting disease progression, using multiomics data to interpret the model. This study enrolled CD patients who underwent baseline testing (including neuroimaging, psychological scales, MR enterography, and ileocolonoscopy) and faecal/blood samples collection. The neurophenotypes of patients were characterized using a neuroimaging-based model. The predictive ability of neurophenotype model for disease progression was evaluated using Cox regression analysis. Multiomics data (including faecal microbiome, faecal/blood metabolomics, intestinal permeability, blood-brain-barrier permeability, and blood neurotransmitter levels) were used to elucidate how neurophenotypes reflect brain-gut interactions.

02

Conditions studied

  • Radiomics
  • Multi-omics

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Keywords

  • Abdominal MRI
  • Magnetic Resonance Imaging
  • Crohn's disease
  • Brain/gut interaction
03

In context

Disease Progression

544 studies on the registry are indexed under Disease Progression; 144 are open to participants now.

This study's planned enrollment of 500 is above the median of 198 across 260 observational studies indexed under Disease Progression.

Browse Disease Progression studies →

Lead sponsor

First Affiliated Hospital, Sun Yat-Sen University is the lead sponsor of 155 studies on the registry; 51 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

This study included adult patients aged 18 to 45 with Crohn's disease (CD) who were admitted to the First Affiliated Hospital of Sun Yat-sen University between May 2021 and June 2025.

Inclusion criteria

  • (a) CD patients aged 18-45 years; (b) the completion of multimodal brain MRI and administration of psychological questionnaires; (c) MR enterography (MRE), ileocolonoscopy, and blood or faecal samples, collection within one week of brain MRI; (d) a follow-up of at least six months for patients without disease progression; and (e) right-handedness.

Exclusion criteria

Exclusion Criteria:

  • (a) recent use of antibiotics, probiotics, or prebiotics within three months prior to inclusion; (b) history of neurosurgery, cerebrovascular disease, or brain trauma; (c) use of central nervous system drugs or antidepressants within three months prior to inclusion; (d) identification of brain lesions on MR scan; (e) claustrophobia; or (f) presence of metal implants.
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Crohn's disease patients with no-to-mild inflammation

    On MR enterography, the Magnetic Resonance Index of Activity (MaRIA) and Magnetic Resonance Enterography Global Score (MEGS) were used to characterize intestinal inflammation by assessing intramural and extramural lesions in both the small and large intestines. In ileocolonoscopy, the Simplified Endoscopic Activity Score for Crohn's Disease (SES-CD) was used to quantify mucosal or luminal lesions from the terminal ileum to the colorectum. Both modalities were used to classify patients with no-to-mild or moderate-to-severe inflammation. We defined patients as having moderate-to-severe inflammation when at least two of the following criteria were met: (1) MaRIA≥11; (2) MEGS≥ 10 for the small bowel or MEGS≥12 for the colon; or (3) SES-CD≥11. Otherwise, patients were categorized as having no-to-mild inflammation.

    Diagnostic Test: Logistic regression (LR) prediction models

  • Crohn's disease patients with moderate-to-severe inflammation

    On MR enterography, the Magnetic Resonance Index of Activity (MaRIA) and Magnetic Resonance Enterography Global Score (MEGS) were used to characterize intestinal inflammation by assessing intramural and extramural lesions in both the small and large intestines. In ileocolonoscopy, the Simplified Endoscopic Activity Score for Crohn's Disease (SES-CD) was used to quantify mucosal or luminal lesions from the terminal ileum to the colorectum. Both modalities were used to classify patients with no-to-mild or moderate-to-severe inflammation. We defined patients as having moderate-to-severe inflammation when at least two of the following criteria were met: (1) MaRIA≥11; (2) MEGS≥ 10 for the small bowel or MEGS≥12 for the colon; or (3) SES-CD≥11. Otherwise, patients were categorized as having no-to-mild inflammation.

    Diagnostic Test: Logistic regression (LR) prediction models

Interventions

  • Diagnostic testLogistic regression (LR) prediction models

    Logistic regression model was used to establish a model to distinguish different levels of intestinal inflammation.

06

What researchers measure

Primary outcomes

  1. The area under the ROC curve (AUC) to assess the performance of diagnostic model

    After baseline brain MRI scanning, patients were followed up.

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • XploreMET v3.0 system
    Shanghai, China
    • Xuehua Li · Contact
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — Disclosure is subject to application

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 11, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06452550
Lead sponsor
First Affiliated Hospital, Sun Yat-Sen University
Responsible party
Xuehua Li (associate chief physician, First Affiliated Hospital, Sun Yat-Sen University) — Principal investigator
First posted
Jun 11, 2024
Start date
May 1, 2021
Primary completion
Jun 1, 2025 (estimated)
Completion
Jun 1, 2025 (estimated)
Last update
Jun 11, 2024

Study contacts

Xuehua Li
Contact
lxueh@mail.sysu.edu.cn
13580364103
Ruonan Zhang
Contact
zhangrn25@mail2.sysu.edu.cn
15124748450
Xuehua Li
principal investigator · Sun Yat-sen University First Affiliated Hospital Department of Radiology

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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