Diagnostic Value of Deep Learning-Based Rapid MRI in Preoperative Evaluation of Acute Cholecystitis

April 18, 2026 updated by: Weibin Wang, Peking Union Medical College Hospital

Fast Abdominopelvic MRI With Deep Learning-Based Reconstruction Algorithm: Image Quality Evaluation and Application in Patients With Common Abdominal and Pelvic Diseases

This is a single-center, prospective observational study at Peking Union Medical College Hospital. The main goal is to evaluate the image quality and clinical value of a new fast abdominopelvic MRI sequence that uses deep learning-based reconstruction.

The study will include adult patients (18 years or older) who need an MRI scan of the abdomen or pelvis as part of their routine care. These patients will receive both the standard MRI sequence and the new fast sequence, with the goal of comparing the two. The fast sequence is designed to be shorter (5-8 minutes) while maintaining or improving image quality, which can help reduce patient discomfort and motion-related artifacts.

Radiologists will assess the quality of the images from both sequences. The study will also look at how well the fast sequence can detect common abdominal and pelvic diseases, such as gallstones, inflammation, and tumors. This study does not involve new drugs, invasive procedures, or changes to standard care. No additional risks to patients are expected beyond those of a standard MRI scan.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100730
        • Recruiting
        • Peking Union Medical College Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The study population consists of adult patients (aged 18 years and older) with clinically suspected acute calculous cholecystitis, who are admitted to Peking Union Medical College Hospital and planned for cholecystectomy. All patients will undergo preoperative fast MRI with deep learning reconstruction for risk stratification and severity grading. Patients with absolute MRI contraindications or non-biliary causes of abdominal pain are excluded.

Description

Inclusion Criteria:

  • Age ≥ 18 years
  • Clinical indication for abdominopelvic MRI examination
  • Able to understand and sign the informed consent form
  • Able to lie supine and cooperate with breath-holding/respiratory commands during MRI

Exclusion Criteria:

  • Presence of absolute contraindications to MRI (e.g., pacemaker, ferromagnetic foreign body, severe claustrophobia)
  • Inability to complete the MRI scan due to severe pain, instability, or altered mental status
  • Pregnant or breastfeeding women (unless explicitly approved by protocol)
  • Previous abdominal/pelvic surgery with contraindications to MRI sequences

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Patients Undergoing Fast Abdominopelvic MRI
Adult patients (≥18 years) with clinical indications for abdominopelvic MRI, who will undergo both standard MRI and fast MRI with deep learning-based reconstruction. The primary focus is to evaluate image quality and diagnostic performance of the fast sequence for common abdominal and pelvic diseases.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Image Quality Score of Fast Abdominopelvic MRI With Deep Learning Reconstruction
Time Frame: Immediately after MRI scan completion
Immediately after MRI scan completion

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2024

Primary Completion (Estimated)

August 12, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

April 18, 2026

First Submitted That Met QC Criteria

April 18, 2026

First Posted (Actual)

April 24, 2026

Study Record Updates

Last Update Posted (Actual)

April 24, 2026

Last Update Submitted That Met QC Criteria

April 18, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • I-24PJ1043

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Acute Cholecystitis

Subscribe