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Patient Positioning and Its Influence on BIS, NOL, and Cerebral Oxygenation in Anesthetized Patients

Patient Positioning and Its Influence on BIS, NOL, and Cerebral Oxygenation in Anesthetized Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07013734
Enrollment
71
Registered
2025-06-10
Start date
2026-08-01
Completion date
2027-05-01
Last updated
2026-08-07

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

Conditions

Monitoring of Depth of Anesthesia

Brief summary

The goal of this observational study is to find out how changes in body position during surgery might affect brain monitoring results in patients who are under general anesthesia.The main question it aims to answer is: \- Does patient positioning have an impact on Bispectral Index (BIS) and Nociception Level (NOL) index monitoring (which are values of awareness in anesthesized patients). Participants will undergo their surgery as planned, except for these extra features: * Extra monitors placed to check brain activity, pain response, and brain oxygen levels. * Before and after the surgery, while the patient is asleep, the patient's table will be moved into two different positions for 2 minutes each to see if the values on the monitor change. * Hard data of the monitors will be extracted and analyzed to evaluate any possible correlation between the position of the patient and brain monitoring results. Participants will then have to answer a short questionnaire after surgery about their memories before and after the anesthesia.

Interventions

None listed

Sponsors

Ciusss de L'Est de l'Île de Montréal
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Adult patients above 18 years old able to consent; * Supine or lithotomy positioning during the surgery;

Exclusion criteria

* Patient with Body Mass Index (BMI) ≥ 35; * Patients over 80 years old.

Design outcomes

Primary

MeasureTime frame
Variation in Bispectral Index (BIS)Perioperative period

Secondary

MeasureTime frame
Variation of Nociception Level (NOL) IndexPerioperative period
Variation of the patient's cerebral saturation measured with cerebral oximetryPerioperative period

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026