- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02101242
Regional Cerebral Oxygen Saturation Under General Anesthesia A Pilot Study
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
Conditions
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
- Elevation of systemic arterial pressure by application of vasopressors
- Consideration of systemic (pulse oxymetric) oxygen saturation
- Adjustment of artificial ventilation subject to endexpiratory concentration of carbon dioxide (CO2)
- Transfusion of concentrated red cells in case of Hemoglobin (Hb) <7-9 g/dl
- 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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Berlin, Germany, 10117
- Department of Anesthesiology and Intensive Care Medicine, CCM and CVK, Charité - Universitätsmedizin Berlin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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:
- orthopedic surgery of the shoulder in beach chair position
- gynecological, urological or general surgery in Trendelenburg's position
- 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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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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.
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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.
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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).
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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)
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Regional cerebral oxygen saturation (rSO2) is measured under different body positions for elective surgery
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Duration of elective surgery (an average of 2 hours)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence and severity of postoperative delirium
Time Frame: In the 10 - day postoperative sample period
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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)
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In the 10 - day postoperative sample period
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Incidence and severity of postoperative cognitive dysfunction
Time Frame: In the 10-day postoperative sample period
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Test battery: Verbal Learning Test, Stroop Colour Word Test, Letter Digit Substitution Test, Concept Shifting Test
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In the 10-day postoperative sample period
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Rate of organ complications
Time Frame: In the 10-day postoperative sample period
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In the 10-day postoperative sample period
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Electrical activity of the brain
Time Frame: Duration of elective surgery (an average of 2 hours)
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Electrical activity of the brain is measured by electroencephalogram (EEG-derived) bispectral index (BIS) monitoring
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Duration of elective surgery (an average of 2 hours)
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Somatic cerebral oxygen saturation (sSO2)
Time Frame: Duration of elective surgery (an average of 2 hours)
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Somatic cerebral oxygen saturation (rSO2) of the lower limbs (absolutely and in side comparison) in cardiac surgery patients
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Duration of elective surgery (an average of 2 hours)
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Hospital length of stay
Time Frame: participants will be followed for the duration of hospital stay, an expected average of 4 weeks
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Post-anaesthesia Discharge Scoring System (PADSS)
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participants will be followed for the duration of hospital stay, an expected average of 4 weeks
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ReCOSA
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