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Completed

NCT Number: NCT03161275

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

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

Completed

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Key information

Conditions

Surgical Complications From General Anesthesia Anesthesia; Reaction Brain Diseases Brain Ischemia Cardiovascular Diseases Central Nervous System Diseases Cerebral Ischemia Cerebrovascular Disorders Nervous System Diseases Vascular Diseases

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hopital

Cracow, Małpololskie, 31-501, Poland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • scheduled for major abdominal surgery for at least 2 h
  • under general anesthesia
  • American Society of Anesthesiologists（ASA）physical status : II ~ III
  • Age > 18

Exclusion criteria

  • refuse of patients
  • patient with results of test: "The Mini Mental State Examination"" less then 24 before operation
  • neurosurgery history of patients

Treatment and study plan

Primary outcomes

  1. cerebral saturation

    Time frame: every 5 minutes throughout the surgery

    decreases in cerebral oxygen saturation (rSO2) during the surgery

Secondary outcomes

  1. the Mini Mental State Examination test

    Time frame: Baseline, 4 day after surgery

    to assessing the changes in the patients' cognitive function

Sponsors and collaborators

Lead sponsor

Jagiellonian University

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
May 19, 2017
Registry last updated
May 19, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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