Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
3000

Summary

Conditions
  • Colitis Ulcerative
  • Crohn Disease
  • Inflammatory Bowel Diseases
Type
Observational
Design
Observational Model: CohortTime Perspective: Other

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

This is a non-interventional, retrospective and prospective study of participants with IBD. This study will collect data to provide accurate and comprehensive information related to treatment patterns associated with biologics use or non-biological therapy in participants with moderate to severe UC ...

This is a non-interventional, retrospective and prospective study of participants with IBD. This study will collect data to provide accurate and comprehensive information related to treatment patterns associated with biologics use or non-biological therapy in participants with moderate to severe UC and CD in routine clinical practice. The study will have retrospective data collection from past records of participants within the last 2 years before participant's enrollment. The prospective part of the study will include one year of observation and data collection after the participant's enrollment in the study. The study will enroll approximately 2000 participants. Participants will be enrolled in one of the two groups: UC Participants CD Participants This multi-center trial will be conducted in Russia, Belarus and Kazakhstan. The overall period of observation in this study will be approximately 12 months. Participants will make 2 visits within their routine practice to the clinic after the enrollment into the study including a final visit at Month 12.

Tracking Information

NCT #
NCT03532932
Collaborators
Not Provided
Investigators
Study Director: Medical Director Takeda