Evaluation of the Relationship Between Pouch Function and Pouch Inflammation in Patients with Ulcerative Colitis

Overview

Información sobre este estudio

The purpose of this study is to find out if there is a relationship between pouch function (the ability to completely evacuate or empty the pouch) and the development of inflammation in the pouch.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • 18 years or older
  • Confirmed diagnosis of ulcerative colitis (UC) and a history of total abdominal colectomy (TAC) with ileal pouch anal anastomosis (IPAA)
  • Closure of ileostomy, with reinstitution of fecal stream through the ileal pouch, at least 3 years prior to enrollment in the study
  • Ability to understand study procedures and to comply with them for the entire length of the study.
  • Men and women of reproductive capability will be enrolled.  Contraception is not required, although a negative urine pregnancy test will be required in all women immediately prior to participation in the study.  

Exclusion Criteria:

  • Female patients who are pregnant (a urine pregnancy test will be performed prior to study procedures)
  • Patients who are on blood thinners, unable to hold for 5 days prior to visit 1, per physician
  • Inability or unwillingness of individual or legal guardian/representative to give written informed consent.
  • Patients with symptoms suggestive of active inflammation (increase in bowel frequency > 3 bowel movements over baseline, bleeding, urgency, or fever > 100.5°F)

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Laura Raffals, M.D.

Cerrado para la inscripción

Contact information:

Shawn Haren B.S., C.C.R.C.

(480) 301-6083

Haren.Shawn@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20156048

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