Efficacy of Ustekinumab-based Integrated Medicine Therapy in Patients With Symptomatic Stricturing Crohn's Disease: a Multicenter, Prospective, Observational Cohort Study

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This study intends to select patients with confirmed moderate-to-severe Crohn's disease (CD) and obstructive symptoms of intestinal stenosis, who have clear evidence of lumen stenosis caused by the disease itself through radiography or endoscopy. After the informed consent of the patients, comprehensive drug therapy with ustekinumab as the mainstay was performed. The basic information and medical history of the patients were collected, and the treatment process of the patients was followed up and recorded, and the drug regimen was adjusted according to the physician's experience and judgment. At different follow-up time points, blood, feces, tissue and other specimens of patients were collected according to the situation, and gastrointestinal endoscopy, imaging examination, laboratory index examination, self-assessment of subjects' symptoms, and nutritional risk screening were performed on the patients. This study evaluated the CD disease activity, obstructive symptoms, and radiographic or endoscopic remission in patients at different follow-up time points, and comprehensively evaluated the efficacy of ustekinumab in relieving stenotic CD and its related factors.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Clinical diagnosis of moderate to severe Crohn's disease

• Obstructive symptoms within the last eight weeks

• A single or several lumen stricture(s) identified by radiological imaging or endoscopy

• For strictures identified by CT enterograph defined as a lesion with combination of a reduction of luminal narrowing \>50%, an increase in bowel wall thickness \>25% relative to non-affected bowel and pre-stricture dilation \>3.0 cm

• For strictures identified during endoscopic procedure defined by intestinal strictures with a lumen diameter ≤12 mm or even inability to pass the endoscope across the narrowing

Locations
Other Locations
China
Department of Gastroenterology, Seventh Medical Center of PLA Army General Hospital
RECRUITING
Beijing
Department of Gastroenterology, Chongqing Renji Hospital, University of Chinese Academy of Sciences
RECRUITING
Chongqing
Department of Gastroenterology, Sixth Affiliated Hospital, Sun Yat-Sen University
RECRUITING
Guangzhou
Center of Inflammatory Bowel Disease, Department of Gastroenterology, the Second Affiliated Hospital, Zhejiang University School of Medicine
RECRUITING
Hangzhou
Department of Gastroenterology, The First Affiliated Hospital of Zhejiang Chinese Medical University
RECRUITING
Hangzhou
Department of Gastroenterology, Huai'an First People's Hospital
RECRUITING
Huai'an
Department of Gastroenterology, Second Affiliated Hospital of Soochow University
RECRUITING
Suzhou
Department of Gastroenterology, Affiliated Hospital of Yangzhou University
RECRUITING
Yangzhou
Contact Information
Primary
Yan Chen, MD.
chenyan72_72@zju.edu.cn
+86-571-87783777
Backup
Jingwen Liu, MD.
jingwen@zju.edu.cn
+86-571-87767061
Time Frame
Start Date: 2024-08
Estimated Completion Date: 2027-08
Participants
Target number of participants: 239
Treatments
patients with symptomatic stricturing Crohn's disease
The decision to start ustekinumab was at the discretion of the treating physician. The initial intravenous (IV) infusion with ustekinumab at baseline was weight-adjusted (260 mg ≤55 kg, 390 mg between 55 and 85 kg, 520 mg ≥85 kg). According to the label, the first subcutaneous (SC) 90 mg induction dose was administered at week 8 followed by a maintenance dose of 90 mg SC every 8 or 12 weeks, at the discretion of the physician.
Sponsors
Collaborators: The First Affiliated Hospital of Zhejiang Chinese Medical University, Yangzhou University, Chongqing Renji Hospital, University of Chinese Academy of Sciences, Sixth Affiliated Hospital, Sun Yat-sen University, First People's Hospital of Hangzhou, Second Affiliated Hospital of Soochow University, Xian-Janssen Pharmaceutical Ltd., Seventh Medical Center of PLA Army General Hospital
Leads: Second Affiliated Hospital, School of Medicine, Zhejiang University

This content was sourced from clinicaltrials.gov