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临床试验/CTRI/2026/03/106766
CTRI/2026/03/106766尚未招募不适用

Upadacitinib in moderate to severe crohns disease who have failed or are intolerant to conventional therapy or biologics therapy: a real world experience from a single tertiary centre

IPGMER, Kolkata1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2026年4月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
92
试验地点
1

研究概览

简要总结

In this study we will acquire the real-world data on the safety and efficacy of Upadacitinib in the management of Crohn’s disease at a single tertiary care center at IPGMER & SSKM Hospital. We will evaluate the clinical response of CD patients to Upadacitinib who are refractory/intolerant to conventional or biological therapy in a real-world setting. We will also evaluate the safety and tolerability of Upadacitinib in CD patients. We will also identify the baseline predictors for therapeutic response to Upadacitinib. Appropriate statistical analysis shall be applied. After applying proper inclusion and exclusion criteria, we shall enroll subjects in our study. Duration of enrollment of  study will be till  May month of 2027.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • male and female with confirmed diagnosis of crohns disease.
  • with inadequate response or intolerant to one or more conventional therapy.

排除标准

  • 未提供

研究者

发起方
IPGMER, Kolkata
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Sumeet Chatterjee

IPGMER, Kolkata

研究点 (1)

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