Colorectal Cancer and Peripheral Neuropathy Study

Overview

Información sobre este estudio

The purpose of this study is to prospectively evaluate the development of neuropathy symptoms and corresponding changes in physical function in persons receiving oxaliplatin based chemotherapy.

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.

  • Patients must be adults, over the age of 18.
  • English speaking.
  • Scheduled to receive at least 3 months of oxaliplatin based chemotherapy, with no other highly neurotoxic agents (cisplatin, a taxane, a vinca-alkaloid, thalidomide, or bortezomib).  
  • Patients who are planning to receive oxaliplatin based chemotherapy as part of a clinical trial will not be specifically excluded from participating on this trial.
  • Participants who have medications prescribed for pain or anxiety will be included; however, they will be asked not to take any as needed (prn) pain or anxiety medications for 4 hours prior to QST, unless their pain or anxiety is severe (7 or higher on a scale of 0-10) in order to minimize influence of these medications on results.

Exclusion Criteria. 

  • Patients with pre-existing neuropathy (greater than 2 on a 0-10 scale), major psychiatric condition (bipolar or schizophrenia) or whose prior medical history could interfere with their ability to fulfill study requirements or provide accurate self-report data will be excluded from participation. 
  • Participants will be screened for these conditions by a review of their medical record and by collection of self-reported information.

Eligibility last updated 3/10/22. 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

Cindy Tofthagen, Ph.D., R.N.

Cerrado para la inscripción

Contact information:

Cindy Tofthagen Ph.D., R.N.

(904) 953-1409

Tofthagen.Cindy@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20521242

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