Brain Oxygenation During Prehospital Anesthesia: an Observational Study

NCT04144803 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1300

Last updated 2022-10-28

No results posted yet for this study

Summary

Brain oxygenation of adult patients undergoing prehospital emergency anesthesia is monitored using noninvasive near-infrared spectroscopy. Patients are afterwards interviewed to define neurological outcome to measure quality of life. The purpose of this study is to reveal the risk factors of prehospital anesthesia related cerebral desaturation events (CDE) and to define the association between CDE and survival, neurological outcome or quality of life.

Conditions

  • Critically Ill
  • Major Trauma
  • Anesthesia
  • Emergencies

Interventions

DIAGNOSTIC_TEST

Cerebral near-infrared spectroscopy

Nonin H500 one-channel near-infrared spectroscopy monitor on forehead of the patient from before induction of anesthesia to arrival to hospital

Sponsors & Collaborators

  • FinnHEMS Ltd

    collaborator UNKNOWN
  • Turku University Hospital

    collaborator OTHER_GOV
  • Tampere University Hospital

    collaborator OTHER
  • Oulu University Hospital

    collaborator OTHER
  • Lapland Hospital District

    collaborator UNKNOWN
  • Kuopio University Hospital

    collaborator OTHER
  • Metropolia University of Applied Sciences

    collaborator OTHER
  • Turku University of Applied Sciences

    collaborator UNKNOWN
  • Tampere University

    collaborator OTHER
  • Oulu University of Applied Sciences

    collaborator UNKNOWN
  • Savonia University of Applied Sciences

    collaborator OTHER
  • Helsinki University Central Hospital

    lead OTHER

Principal Investigators

  • Jouni Nurmi, MD, PhD · Helsinki University Central Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-18
Primary Completion
2022-09-25
Completion
2023-12-31

Countries

  • Finland

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 NCT04144803 on ClinicalTrials.gov