Measurement of the Cerebral Saturation for Assessment of Safety of Epidural Anaesthesia During Abdominal Surgery

NCT03161275 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2017-05-19

No results posted yet for this study

Summary

Subsequent and non-randomised patients, adult patients qualified for major abdominal surgeries were enrolled

Conditions

  • Surgical Complications From General Anesthesia
  • Cerebral Ischemia
  • Anesthesia; Reaction

Sponsors & Collaborators

  • Jagiellonian University

    lead OTHER

Principal Investigators

  • Tomasz Składzień, Ph.D · University Hospital in Cracow

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2013-03-31
Completion
2013-04-30

Countries

  • Poland

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 NCT03161275 on ClinicalTrials.gov