Assessment of Peripheral Perfusion in the Critically Ill Patient

NCT02771002 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2017-06-22

No results posted yet for this study

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.

Conditions

  • Peripheral Perfusion

Interventions

DEVICE

Peripheral Perfusion index by Carescape Patientenmonitor

Peripheral Perfusion index measured with pulse-oximetry by Carescape Patientenmonitor

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-07-13
Primary Completion
2017-03-28
Completion
2017-03-28

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02771002 on ClinicalTrials.gov