A 5-year Longitudinal Observational Study of Patients Undergoing Therapy for Inflammatory Bowel Disease

  • STATUS
    Recruiting
  • End date
    Jul 23, 2025
  • participants needed
    15000
  • sponsor
    Target PharmaSolutions, Inc.
Updated on 23 September 2021
Investigator
Laura Dalfonso
Primary Contact
Advanced Gastroenterology Associates, LLC (7.1 mi away) Contact
+36 other location
ulcerative colitis
inflammatory bowel disease
crohn's disease
enteropathy
colitis
ulceration
indeterminate colitis
intestinal diseases

Summary

TARGET-IBD is a 5-year, longitudinal, observational study of adult and pediatric patients (age 2 and above) being managed for Inflammatory Bowel Disease (IBD) in usual clinical practice. TARGET-IBD will create a research registry of patients with IBD within academic and community real-world practices in order to assess the safety and effectiveness of current and future therapies.

Details
Condition Gastroenteritis, Intestinal Diseases, Ulcerative Colitis, Inflammatory bowel disease, Crohn's Disease, Indeterminate Colitis, Crohn's Disease (Pediatric), Ulcerative Colitis (Pediatric), Bowel Dysfunction, inflammatory bowel diseases, crohns disease
Clinical Study IdentifierNCT03251118
SponsorTarget PharmaSolutions, Inc.
Last Modified on23 September 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Adults and children (age 2 or older) with a diagnosis of Crohn's disease (CD), Ulcerative colitis (UC), or Indeterminate colitis (IBDU) having been prescribed any IBD treatment (initial or subsequent) outside of a clinical trial
Have plans for future visits at the site for continued management of IBD

Exclusion Criteria

Inability to provide written informed consent/assent
Being enrolled in any interventional study or trial for IBD treatment. Note: Patient may be enrolled in other registries or studies where IBD treatment outcomes are observed and/or reported (such as center-based registries)
Prior total abdominal colectomy for UC or IBDU
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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