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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorCiusss de L'Est de l'Île de Montréal

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients above 18 years old able to consent;

Supine or lithotomy positioning during the surgery;

Disqualifiers

Patient with Body Mass Index (BMI) ≥ 35;

Patients over 80 years old.

Trial population

Patients from Maisonneuve-Rosemont Hospital undergoing elective surgery.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Variation in Bispectral Index (BIS)

Time frame
Perioperative period

Secondary outcomes

1

Variation of Nociception Level (NOL) Index

Time frame
Perioperative period
2

Variation of the patient's cerebral saturation measured with cerebral oximetry

Time frame
Perioperative period

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: