HIPULSE (Blood Pressure) - Clinical Trial

¿Cuál es el Propósito de este estudio?

We are doing this study to assess how accurately a medical device under test that can measure blood pressure and changes to blood pressure during surgery non-invasively. We want to compare its performance and accuracy to that of an arterial line, which is an invasive procedure.

¿Cuál es la Condición que se está estudiando?

Arterial Blood Pressure Monitoring in the Operating Room or Intensive Care

¿Quién puede participar en el Estudio?

Adults ages 18+ who:

  • Have an upcoming surgery or current or planned stay in the ICU
  • Are not having an emergency surgery
  • Do not have severe aortic or mitral valve dysfunction

For more information, contact the study team at emmalee.metzler@duke.edu.

Grupo etario
Adultos

¿Qué Implica?

If you choose to join this study, we will apply the study device (cuff) to your arm during your surgery or ICU stay, whichever might be applicable. We will collect blood pressure information during this time. We will then remove the device. We will check your arm for any redness, irritation, or issues.

Detalles del Estudio

Título Completo
The HIgh-fidelity hydraulic couPling Upper-arm cuff assessment of Limits, Safety, and Effectiveness (HIPULSE) Trial (Blood Pressure)
Investigador Principal
Especialista en anestesiología
Número de Protocolo
IRB: PRO00118179
NCT: NCT06895590
Fase
Phase II
ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción