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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03161275

Enrollment

101

Registered

2017-05-19

Start date

2012-07-31

Completion date

2013-04-30

Last updated

2017-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

cerebral saturation, epidural anaesthesia, Near Infrared Spectroscopy (NIRS), Regional cerebral oxygen saturation

Brief summary

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

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 100 Years

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
cerebral saturation	every 5 minutes throughout the surgery	decreases in cerebral oxygen saturation (rSO2) during the surgery

Secondary

Measure	Time frame	Description
the Mini Mental State Examination test	Baseline, 4 day after surgery	to assessing the changes in the patients' cognitive function

Countries

Poland

Outcome results