SBOM-AI: Total Small Bowel Length Measurement Using Computed Tomography and Magnetic Resonance Imaging in Obese Patients

Sponsor
University of Roma La Sapienza (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06065917
Collaborator
University of Padova (Other), Federico II University (Other)
195
1
28.1

Study Details

Study Description

Brief Summary

The aim of the study is to set up and validate a reliable and reproducible automated method using preoperative radiological imaging to measure the TSBL in patients undergoing laparoscopic bariatric/metabolic surgery.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Measurement of the total small bowel length using CT scan and MRI with 3D reconstruction and AI tool
N/A

Detailed Description

The total length of the small intestine (TSBL) represents a crucial parameter for obtaining a safe and successful minimally invasive surgery in metabolic/bariatric bypass surgery.

Nowadays, the standard of small intestine measurement is the intraoperative measurement. Laparoscopy represents the standard approach for baratric/metabolic, making the TSBL measurement time-consuming and risky in case of intestinal lesions. An accurate and effective non-invasive preoperative measurement of the TSBL will allow to evaluate the variability of the TSBL, which affects the surgical strategy. Cross-sectional imaging could play an important role in this setting thanks to the possibility of measuring in a non-invasive way the TSBL. Some studies performed with both Computed Tomography (CT) and Magnetic Resonance (MR) report promising results. However, they are limited by the small size of the sample, the lack of standardized technique and the lack of an automatic method based on Artificial Intelligence (AI).

The evaluation of a reliable preoperative method to measure TSBL using cross-sectional imaging will potentially reduce intraoperative complications and insufficient long-term weight loss or nutritional deficiencies. In this scenario a possible solution could be the implementation of analysis method through the development of an AI algorithm capable of automatically segmenting the small intestine.

The PRIMARY END POINT of this study is to set up and validate a reliable and reproductible automatic method to measure the TSBL in patients candidates for laparoscopic bariatric/metabolic surgery, based on preoperative radiological imaging

The main phases of the project will be:
  1. evaluate the feasibility of preoperative CT and MRI-base measurement of the TSBL in a large cohort of obese patients and compare radiological measurement with intraoperative laparoscopic measurement (method of elongation) as a reference standard (1).

  2. Evaluate the more accurate cross-sectional imaging between CT and MRI to measure the length of the small intestine.

  3. Build an AI tool that can automatically measure TSBL on transversal slice imaging.

Three high-volume Italian centers will enroll 195 obese patients who are candidates for metabolic surgery for obesity. Part of them will be established training cohort (total = 105 patients), used to set up the AI-based method of TSBL measurement. The other 90 patients (30 for each center) will represent the validation cohort.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
195 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Set up and Validation of Total Small Bowel Length Measurement Using Computed Tomography and Magnetic Resonance Imaging With 3D Reconstruction and Artificial Intelligence Tool in Obese Patients Candidates to Metabolic Surgery
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Nov 1, 2025
Anticipated Study Completion Date :
Feb 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Artificial intelligence training cohort and validation cohort

Three high-volume Italian centers will enroll 195 obese patients who are candidates for metabolic surgery for obesity. Part of them will be established a training cohort (total = 105 patients), used to set up the AI-based method of TSBL measurement. The other 90 patients (30 for each center) will represent the validation cohort.

Diagnostic Test: Measurement of the total small bowel length using CT scan and MRI with 3D reconstruction and AI tool
The intervention consists in performing CT and MR imaging with small bowel length measurement before bariatric/metabolic surgery in obese patients. Then, during surgery the patients will undergo laparoscopic stretched small bowel measurement as the reference gold standard method to measure the small bowel length. The imaging of the training cohort will be used to trained an AI to set up an automatic method of small bowel length measurement via the analysis of CT and MRI imaging.

Outcome Measures

Primary Outcome Measures

  1. Concordance between AI-based total small bowel length measure and laparoscopic total small bowel length measure [1 month]

    the main outcome is to set up and validate a reliable and reproducible automated method using preoperative radiological imaging to measure the TSBL in patients candidates for laparoscopic bariatric/metabolic surgery. The results of AI measurement will be compared with those of laparoscopic measurement to examine the level of concordance

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • BMI > 35 kg/m2 and at least one obesity-related comorbidity

  • BMI > 40 kg/m2

  • failure of at least six months of dietary and/or medical treatment of obesity

  • indication for intervention validated after multidisciplinary evaluation in a specific board meeting

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Roma La Sapienza
  • University of Padova
  • Federico II University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Niccolo Petrucciani, MD, PhD, Associate Professor of Surgery, University of Roma La Sapienza
ClinicalTrials.gov Identifier:
NCT06065917
Other Study ID Numbers:
  • C.88
First Posted:
Oct 4, 2023
Last Update Posted:
Oct 4, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Niccolo Petrucciani, MD, PhD, Associate Professor of Surgery, University of Roma La Sapienza
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 4, 2023