A Study to Evaluate the Use of a Novel Wearable Device for Temperature Monitoring in Cancer Patients Who Underwent Autologous Stem Cell Transplant

Overview

Información sobre este estudio

The purpose of this study is to evaluate the performance of the wearable tPatch device when compared to an oral temperature measuring device in patients who have undergone a post-autologous bone marrow transplant.

 

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:

  1. Subjects at least 18 years of age
  2. Subjects able to read, understand, and complete the informed consent form
  3. Subjects treated for cancer and scheduled to undergo autologous stem cell transplant at Mayo Clinic, Rochester, MN
  4. Subjects able to wear wearable temperature sensing device(s) for the duration of the study
  5. Subjects able to record body temperature per the protocol for the duration of the study

Exclusion Criteria:

  1. Subjects pregnant or breastfeeding
  2. Subjects with leukemia
  3. Subjects diagnosed with renal failure based on estimated glomerular filtration rate (eGFR) for age, size, gender and race norms
  4. Subjects with ECOG performance status of 2 and greater
  5. Subjects with known allergies to medical grade adhesives
  6. Subjects with known cutaneous hypersensitivity
  7. Subjects with impaired decision-making capabilities
  8. Subjects with wireless medical devices or implantable electronic medical devices (e.g., pacemakers, implantable defibrillators, and spinal stimulators)
  9. Subjects febrile at time of enrollment or placement of the tPatch device
  10. Any additional condition or situation that, in the opinion of the Investigator, makes the subject inappropriate for participation in the study

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

Rochester, Minn.

Investigador principal de Mayo Clinic

Svetomir Markovic, M.D., Ph.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20426329

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