Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT07093294

Value of IUS in Predicting Vedolizumab Efficacy and Assessing Transmural Healing in Early Crohn's Disease: A Multicenter, Prospective Study

Led by The Third Xiangya Hospital of Central South University · Updated on 2025-07-30

60

Participants Needed

1

Research Sites

121 weeks

Total Duration

On this page

Sponsors

T

The Third Xiangya Hospital of Central South University

Lead Sponsor

T

The First Affiliated Hospital of University of South China

Collaborating Sponsor

AI-Summary

What this Trial Is About

Crohn's disease(CD) is a chronic nonspecific inflammatory disease of the intestinal tract whose etiology is not yet fully understood,characterized by transmural inflammation , can present with serious complications such as intestinal obstruction, perforation, abdominal abscesses, and fistulae. In recent years, the incidence of CD has increased rapidly, causing a heavy social and economic burden. Currently, the main therapeutic drugs for CD include aminosalicylic acid preparations, glucocorticoids, immunosuppressants, and biological agents. With the development of medical technology, small molecule preparations have begun to be applied to moderate-to-severe Crohn's disease, providing new treatment options for patients with Crohn's disease. Vedolizumab, a humanized monoclonal antibody.the GEMINI study demonstrated its superior efficacy over placebo in inducing and maintaining clinical remission. And the VERSIFY study confirmed its advantage in achieving mucosal healing, with a transmural healing rate of 29.1% at week 52. Intestinal ultrasound is a noninvasive, reproducible, convenient, and inexpensive test that can greatly increase the frequency of assessing treatment response and speed up the clinical decision-making process.The 2019 ECCO-ESGAR guidelines recommend intestinal ultrasound for disease monitoring in patients with CD. Multiple studies have shown that most ultrasound markers normalize within 12 weeks of treatment initiation, and in particular, normalization of bowel wall thickness is highly correlated with clinical response at 12 weeks. There are no validated indicators to predict the efficacy of upadacitinib treatment in patients with moderate-to-severe CD in the currently available studies. Currently, there are no national or international studies in which intestinal ultrasound predicts the efficacy and assesses the transmural healing of vedolizumab therapy. Therefore, we propose for the first time that intestinal ultrasound be used as a method to predict the response to vedolizumab in early CD patients, with the aim of providing evidence to guide the development of individualized treatment plans.

CONDITIONS

Official Title

Value of IUS in Predicting Vedolizumab Efficacy and Assessing Transmural Healing in Early Crohn's Disease: A Multicenter, Prospective Study

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years and older and 80 years and younger
  • Patients with early Crohn's disease diagnosed within 18 months
  • No previous biologic or advanced therapy treatments
  • Vedolizumab treatment planned within 1 month after baseline endoscopy and ultrasound
  • No history of intestinal surgery
  • Able to understand and voluntarily consent to participate in the study
Not Eligible

You will not qualify if you...

  • Allergy or contraindications to vedolizumab
  • Active tuberculosis or other active infections
  • Moderate-to-severe heart failure (NYHA grade III or IV)
  • Demyelinating nervous system diseases
  • Live vaccination within the last 3 months
  • Pregnancy or breastfeeding
  • History of extensive colectomy or planned colectomy
  • History of colonic mucosal dysplasia
  • Hypersensitivity to SonoVue contrast media

AI-Screening

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Trial Site Locations

Total: 1 location

1

The Third Xiangya Hospital of Central South University

Changsha, Hunan, China, 410000

Actively Recruiting

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Research Team

T

Tian Li

CONTACT

Y

Yuwei Wu

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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