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The Effects of Demographic and Clinical Data of Patients on Cerebral Oxygen Monitoring Values

The Effects of Demographic and Clinical Data of Patients on the Assessment of Cerebral Oxygen Monitoring Values Applied During Coronary Artery Bypass Grafting

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07228546
Enrollment
80
Registered
2025-11-14
Start date
2025-05-12
Completion date
2025-12-31
Last updated
2026-01-07

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

Conditions

Cerebral Oxygen Saturation

Keywords

near infrared spectroscopy, coronary artery bypass grafting, regional cerebral oxygen saturation

Brief summary

The aim of this study is to examine the effects of patients' clinical and demographic datas on cerebral oxygen saturation values. Brain oxygenation is measured using near infrared spectroscopy (NIRS). The primary outcome measure of the study is the regional oxygen saturation (rSO2) values measured on the monitor at twelve time points. The other primary outcome measures consist of baseline arterial and venous blood gas analysis and baseline activated clotting time measurements.

Detailed description

This prospective observational study analyzes 80 patients between the ages of 25-80 years who are undergoing elective coronary artery bypass grafting (CABG) surgery. Demographic data of the patients such as age, gender, comorbidities, body mass index are recorded. In addition to standard monitoring, cerebral oximetry monitoring (NIRS) is applied to the patients. Baseline arterial and venous blood gas analysis values, baseline activated clotting time measurements are recorded. Durations of anesthesia, surgery , cardiopulmonary bypass , aortic cross- clamping are recorded. Time points for rSO2 values are baseline, induction, sternotomy, cannulation, pump entry, cross clamp placement, 34º C ,36º C, lowest temperature, cross clamp removal, pump exit, skin closure.

Interventions

None listed

Sponsors

Tuna Şahin
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
25 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Accepting to participate in the study * Undergoing elective coronary artery bypass grafting surgery * Age 25-80 years Ejection fraction 30% and above

Exclusion criteria

* Non volunteers * Age \<25 or \>80 years * Ejection fraction below 30% * Patients with history of neurological disease or neurosurgery * Emergency surgery * Concurrent valve surgery * Patients with history of carotid artery stenosis * Patients with need for preoperative intraaortic balloon pump or inotropic support

Design outcomes

Primary

MeasureTime frameDescription
Regional oxygen saturation valuesBaseline and peroperative measurements until the and of surgeryRegional oxygen saturation values measurement at twelve points.
Baseline arterial blood gas analysisWithin 5 minutes after arterial cannulation for the baseline measurementThe baseline arterial blood gas sample taken from the patient after arterial cannulation
Venous blood gas analysisWithin 5 minutes after central jugular venous cannulationVenous blood gas sample taken from the patient after central jugular venous cannulation
Baseline activated clotting time measurementWithin 5 minutes after arterial cannulation for the baseline measurementThe baseline measurement of activated clotting time after arterial cannulation

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026