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A Study to Develop a Registry for Outcomes and Predictors in Pouch-Related Disorders

Overview

About this study

The primary purpose of this study is to create a prospective registry of patients with pouch-related conditions to allow for longitudinal assessment of outcomes at 3, 6 and 12 months after a enrollment with a specific diagnosis (acute pouchitis, CADP, CARP, or CD of the pouch).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients with pouch-related disorders will be recruited from participating sites at the time of clinic visits.
  • At the time of enrollment, patients will be classified as having one of four inflammatory pouch conditions (acute pouchitis, CADP, CARP, or CD of the pouch).
  • All visits will be standard of care visits, where patients are identified as potential candidates for enrollment based on presentation with a pouch-related diagnosis.
  • Following the initial recruitment and data collection, patients will complete online questionnaires at 3, 6, and 12 months following enrollment in the prospective pouch registry.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Laura Raffals, M.D.

Open for enrollment

Contact information:

Chad Rypstra

(507)538-4289

Rypstra.Chad@mayo.edu

More information

Publications

Publications are currently not available

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CLS-20467374

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