PAtient-CenTric Chronic Pancreatitis Registry (PACT-CP)

Overview

Información sobre este estudio

The main objective of this study is to generate real-world evidence reflecting the experience of individuals with exocrine pancreatic insufficiency (EPI) due to chronic pancreatitis (CP). Efforts will be directed toward understanding the unmet need and therapeutic burden to identify the most critical factors that influence treatment choices/prescribing patterns, quality of life, and healthcare utilization outcomes in standard of care for individuals with EPI due to CP.

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:

  • At least 18 years of age (or age of majority).
  • Willing to provide consent to participate.
  • Meet ONE (1) of the following at the time of enrollment:
    • Diagnosis of chronic pancreatitis (CP);
    • Diagnosis of recurrent acute pancreatitis (RAP).
  • Suspected or confirmed diagnosis of EPI made by a healthcare provider.
  • On PERT, either prior to the Enrollment Visit or newly prescribed at the time of the Enrollment Visit.

Exclusion Criteria:

  • Currently participating in or planning to participate in a double-blind randomized trial and/or open-label Phase 3b/4 on CP or EPI.
  • Diagnosed with any of the following conditions at the time of enrollment:
    • Cystic fibrosis;
    • Fibrosing colonopathy;
    • A history of or current diagnosis of pancreatic cancer, main duct papillary mucinous neoplasms (IPMNs), and other pancreatic malignancies;
    • Allergy to pork or other porcine pancreatic enzyme products (PEPs);
    • Any condition that would, in the investigator’s opinion, limit the individual’s ability to complete the study.

Eligibility last updated 9/24/21. Questions regarding updates should be directed to the study team contact.

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

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Jane Diamond, APRN

Cerrado para la inscripción

Contact information:

Guillermo Pradieu M.P.H.

Pradieu.Guillermo@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20539654

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