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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04999228
Other study ID # UC1.1
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date November 1, 2021
Est. completion date December 31, 2026

Study information

Verified date February 2024
Source Children's Hospital of Fudan University
Contact Cui fang Zheng
Phone 8615221881022
Email zhengcuifang2@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pediatric Ulcerative Colitis (UC) patients with moderate to severe disease activity at high risk of colectomy. Early use of biologic agents will likely be more effective. But there were no studies identified that compared a strategy of upfront biologic-based therapy versus gradual step-up therapy. In our study, newly diagnosed moderate to severe pediatric UC patients (6-18 years old) will be randomly divided into infliximab (IFX) treatment group (Top down group, TD) and corticosteroids (CS) treatment group (Step-up group, SU). Mucosal healing rate at week 12 will be compared between the two groups. The relapse rates and sustained durations of remission within one year will also be evaluated.


Description:

Pediatric ulcerative colitis (UC) is typically more extensive and has a more active disease course than adult UC. Pediatric UC patients with moderate to severe disease activity at high risk of colectomy. Rapid disease control may improve the prognosis of the disease and reduce the rate of surgery. Early use of biologic agents will likely be more effective. But there were no studies identified that compared a strategy of upfront biologic-based therapy versus gradual step-up therapy. In our study, newly diagnosed moderate to severe pediatric UC patients (6-18 years old) will be randomly divided into infliximab (IFX) treatment group (Top down group, TD) and corticosteroids (CS) treatment group (Step-up group, SU). A decrease of pediatric ulcerative colitis activity index (PUCAI) at least 20 points were defined as Clinical response. Clinical response will be evaluated at week 2 in SU group and week 6 in TD group. For no-responder, treatment plan will be changed. Clinical remission rate at week 10 and mucosal healing rate at week 12 will be compared between the two groups. The relapse rates and sustained durations of remission within one year will also be evaluated.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 31, 2026
Est. primary completion date June 1, 2025
Accepts healthy volunteers No
Gender All
Age group 6 Years to 18 Years
Eligibility Inclusion Criteria: 1. newly diagnosed UC; 2. moderate to severe disease activity 3. Age: 6 to 18 years old Exclusion Criteria: 1. with mild disease activity 2. Have been treated with Corticosteroid or biological agents for UC

Study Design


Intervention

Drug:
Infliximab
Infliximab will be administered intravenously at a dose of 5 mg/kg for 0, 2, and 6 weeks, then every 8 weeks for 1 year.
Corticosteroids
Corticosteroid will be given at a dose of 1-2mg/kg/day (maximum 60 mg/kg/day),oral or intravenously for 12 to 14 weeks.

Locations

Country Name City State
China Children's Hospital of Fudan University Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital of Fudan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mucosal healing rate The Ulcerative Colitis Endoscopic Index of Severity (UCEIS) ?1 points is defined as mucosal healing. This will be evaluated by inflammatory bowel disease endoscopist. 12 week after intervention
Secondary The relapse rates Relapse is defined as an increased in pediatric Ulcerative Colitis activity index (PUCAI) score by 10 points or more after clinical remission or when new Ulcerative Colitis treatment needed to be started due to worsening of symptoms. This will be evaluated by gastroenterologist. 1 year after intervention
Secondary Sustained durations of remission Sustained pediatric Ulcerative Colitis activity index (PUCAI) score <10 points during follow-up(week 10 to week 54 after intervention). This will be evaluated by gastroenterologist. 1 year after intervention
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