Clinical Trials Directory

Trials / Completed

CompletedNCT02771002

Assessment of Peripheral Perfusion in the Critically Ill Patient

Evaluation of the Clinical Assessment of Peripheral Perfusion by Capillary Refill Time and Peripheral Perfusion Index

Status
Completed
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
Insel Gruppe AG, University Hospital Bern · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate PPI as a surrogate for clinical signs of peripheral perfusion in patients in septic shock and after cardiac surgery.

Detailed description

The aim of this study is to validate PPI as a continuous, objective measurement of peripheral perfusion indicated by clinical sings of tissue perfusion in patients with septic shock. Furthermore, PPI shall be compared to the perfusion of solid organs evaluated by ultrasound of liver, kidney and gut. In a group of healthy volunteers the investigators will determine normal values in ambient temperature and after cooling of an extremity. Another group of patients after cardiac surgery, where usually a poor tissue perfusion without metabolic failure is present will serve as another "control" population in their post-surgery stabilization period. The values from healthy volunteers and cardiac surgery patients will be compared to those of patients in septic shock.

Conditions

Interventions

TypeNameDescription
DEVICEPeripheral Perfusion index by Carescape PatientenmonitorPeripheral Perfusion index measured with pulse-oximetry by Carescape Patientenmonitor

Timeline

Start date
2016-07-13
Primary completion
2017-03-28
Completion
2017-03-28
First posted
2016-05-12
Last updated
2017-06-22

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02771002. Inclusion in this directory is not an endorsement.