Regional Cerebral Oxygen Saturation Under General Anesthesia A Pilot Study

June 26, 2019 updated by: Claudia Spies, Charite University, Berlin, Germany

A total of 60 patients will be enrolled in the study: 20 each who receive surgery in beach chair position or Trendelenburg's position and 20 patients undergoing cardiac surgery. Regional cerebral oxygen saturation will be measured continuously during surgery. Duration and extent of deviations from individual baseline values will be recorded and detected deviations treated according to their clinically apparent cause (e.g. hypotension/hypovolaemia, anaemia, low cardiac output) in accordance with our standard operating procedures (SOPs).

Patients are then followed up until the end of hospital stay or for a maximum of 10 days after surgery. Their level of cognitive function will be tested and compared to the data acquired before surgery to detect impairment, delirium or postoperative cognitive deficit (POCD).

The purpose of this pilot study is to evaluate the design and conduct of a projected full scale observational clinical study.

Study Overview

Status

Terminated

Detailed Description

The primary goal of this study is the detection of perioperative fluctuations of regional cerebral oxygen saturation in patients undergoing surgery in general anaesthesia. These fluctuations will be monitored using the a non-invasive monitoring system based on the method of near-infrared spectroscopy (NIRS).

Regional cerebral hypoxia is considered one of the possible precipitating factors of postsurgical cognitive impairment (as seen in patients with postoperative cognitive deficit or postoperative delirium), but without monitoring it may easily remain undetected. A differentiated analysis of fluctuations is gained by calculation of the area under curve (AUC) of a defined deviation from individual baseline regional cerebral oxygen saturation (rSO2) over time.

When deviations are detected, they will be treated in this study according to their clinically apparent cause (e.g. hypotension/hypovolaemia, anaemia, low cardiac output) in accordance with current standard operating procedures (SOPs) to re-elevate regional cerebral oxygen saturation (rSO2) to within 20% of baseline.

Among these procedures are

  1. Elevation of systemic arterial pressure by application of vasopressors
  2. Consideration of systemic (pulse oxymetric) oxygen saturation
  3. Adjustment of artificial ventilation subject to endexpiratory concentration of carbon dioxide (CO2)
  4. Transfusion of concentrated red cells in case of Hemoglobin (Hb) <7-9 g/dl
  5. Transthoracic or transesophageal echocardiogram (TTE/TEE) and assessment of centralvenous oxygen saturation in case of suspected myocardial insufficiency

which should be applied to patients of the 3 defined groups as needed.

This explorative project is a pilot study.

Study Type

Observational

Enrollment (Actual)

42

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Berlin, Germany, 10117
        • Department of Anesthesiology and Intensive Care Medicine, CCM and CVK, Charité - Universitätsmedizin Berlin

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients of both genders, over 18 years of age, undergoing elective surgery in general anesthesia.

Description

Inclusion Criteria:

  • patients with male-to-female ratio approaching 1:1
  • age ≥ 18 years
  • scheduled duration of surgery longer than or equal to 60 minutes
  • patients undergoing one of the following procedures:

    1. orthopedic surgery of the shoulder in beach chair position
    2. gynecological, urological or general surgery in Trendelenburg's position
    3. cardiac surgery

Exclusion Criteria:

  • Moribund patients
  • Persons without the capacity to consent
  • Unability of German language use
  • Inability of communication due to severe hearing and severe vision impairments
  • Accommodation in an institution due to an official or judicial order
  • Co-worker of the Charité
  • Participation in another interventional study within 30 days before participation in this study
  • Alcohol- use disorders according to the Alcohol Use Disorders Identification Test (AUDIT)
  • Preoperative Dementia (Minimal Mental State Examination < 24)
  • Stroke, traumatic brain injury within the last 12 months or patients with residual neurological deficits

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Orthopedic surgery of the shoulder
Near-infrared spectroscopy (NIRS) can detect fluctuation of regional cerebral oxygen saturation during change from supine position to beach chair position.
Gynecological, urological or general surgery
Near-infrared spectroscopy (NIRS) can detect fluctuation of regional cerebral oxygen saturation during change from supine position to Trendelenburg position.
Cardiac surgery
Near-infrared spectroscopy (NIRS) can detect fluctuation of regional cerebral oxygen saturation in patients undergoing cardiac surgery with cardiopulmonary bypass (heart-lung machine).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Regional cerebral oxygen saturation (rSO2)
Time Frame: Duration of elective surgery (an average of 2 hours)
Regional cerebral oxygen saturation (rSO2) is measured under different body positions for elective surgery
Duration of elective surgery (an average of 2 hours)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence and severity of postoperative delirium
Time Frame: In the 10 - day postoperative sample period
Nursing Delirium Screening Scale (Nu-DESC), Confusion Assessment Method (CAM-ICU), Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-V) (DSM-V), International Classification of Diseases (ICD)-10 (ICD-10)
In the 10 - day postoperative sample period
Incidence and severity of postoperative cognitive dysfunction
Time Frame: In the 10-day postoperative sample period
Test battery: Verbal Learning Test, Stroop Colour Word Test, Letter Digit Substitution Test, Concept Shifting Test
In the 10-day postoperative sample period
Rate of organ complications
Time Frame: In the 10-day postoperative sample period
In the 10-day postoperative sample period
Electrical activity of the brain
Time Frame: Duration of elective surgery (an average of 2 hours)
Electrical activity of the brain is measured by electroencephalogram (EEG-derived) bispectral index (BIS) monitoring
Duration of elective surgery (an average of 2 hours)
Somatic cerebral oxygen saturation (sSO2)
Time Frame: Duration of elective surgery (an average of 2 hours)
Somatic cerebral oxygen saturation (rSO2) of the lower limbs (absolutely and in side comparison) in cardiac surgery patients
Duration of elective surgery (an average of 2 hours)
Hospital length of stay
Time Frame: participants will be followed for the duration of hospital stay, an expected average of 4 weeks
Post-anaesthesia Discharge Scoring System (PADSS)
participants will be followed for the duration of hospital stay, an expected average of 4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 11, 2014

Primary Completion (ACTUAL)

September 14, 2014

Study Completion (ACTUAL)

September 17, 2014

Study Registration Dates

First Submitted

March 13, 2014

First Submitted That Met QC Criteria

March 28, 2014

First Posted (ESTIMATE)

April 2, 2014

Study Record Updates

Last Update Posted (ACTUAL)

June 28, 2019

Last Update Submitted That Met QC Criteria

June 26, 2019

Last Verified

June 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • ReCOSA

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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