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Effect of Operating Room Noise on BIS and Hemodynamics Under General Anesthesia

The Effect of Operating Room Environmental Noise on BIS and Hemodynamics in Patients Under General Anesthesia: A Prospective Observational Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07194707
Enrollment
70
Registered
2025-09-26
Start date
2026-08-01
Completion date
2026-12-01
Last updated
2026-07-22

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

Conditions

General Anesthesia, Hemodynamics, Noise Exposure

Keywords

Anesthesia, General, Operating Rooms, Monitoring, Intraoperative, Hemodynamics, Bispectral Index (BIS), Noise Exposure

Brief summary

This prospective observational study aims to evaluate the impact of operating room noise on bispectral index (BIS) and hemodynamic parameters in patients undergoing general anesthesia. Environmental noise in operating rooms, often overlooked, may influence anesthesia depth, patient safety, and physiological stability. A total of 70 adult patients (ASA I-II, 18-65 years, elective surgery under general anesthesia) will be enrolled at Başakşehir Çam and Sakura City Hospital. Patients will be categorized into two groups based on intraoperative average noise levels: noisy group (\>65 dB) and quiet group (\<55 dB). Noise levels will be measured every 10 minutes using a CEM DT-8850 sound level meter, BIS will be recorded every 10 minutes, and hemodynamic variables (systolic, diastolic, mean arterial pressure, and heart rate) will be recorded every 5 minutes. Primary outcome is the correlation between mean intraoperative noise levels (LAeq) and BIS values during the maintenance phase of anesthesia. Secondary outcomes include the relationship between noise characteristics (e.g., device-related, human-related, alarms, media) and hemodynamic stability, as well as surgical branch-related noise classifications (high, moderate, low). The study is non-interventional, with no additional risk to participants beyond standard clinical monitoring. Findings are expected to provide evidence on the role of environmental noise in anesthesia quality, inform operating room organization, and contribute to patient safety improvements.

Detailed description

Operating room (OR) noise is a common but underestimated environmental factor that may affect both patients and medical staff. In patients under general anesthesia, excessive noise may influence depth of anesthesia, physiological stability, and recovery outcomes.This prospective observational study will investigate the correlation between intraoperative noise levels and bispectral index (BIS) values, as well as hemodynamic parameters (systolic, diastolic, and mean arterial pressure, and heart rate). Seventy adult patients undergoing elective surgery under general anesthesia will be monitored. Noise levels will be measured every 10 minutes with a calibrated sound level meter (CEM DT-8850), while BIS and hemodynamic parameters will be recorded at 10-minute and 5-minute intervals, respectively. Additionally, the type of noise (device-related, human-related, alarms, media) and the surgical branch (classified into high, moderate, or low noise categories) will be documented. Data will be analyzed to determine whether environmental noise correlates with BIS fluctuations and hemodynamic stability. The study is observational only and involves no intervention beyond standard anesthesia practice. Results are expected to raise awareness of environmental influences on anesthesia management and provide recommendations for OR organization to enhance patient safety.

Interventions

OTHERIntraoperative Noise Monitoring

Noise levels will be passively measured during surgery using a calibrated sound level meter (CEM DT-8850) placed near the patient's head. Measurements will be taken every 10 minutes without physical contact or interference with clinical care. The procedure is purely observational and does not modify anesthesia or surgical practice.

Sponsors

Başakşehir Çam & Sakura City Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 18-70 * ASA (American Society of Anesthesiologists) physical status score I-II * Scheduled for elective surgery * To be undergoing general anesthesia * Having signed the informed consent form to participate in the study

Exclusion criteria

* Hearing impairment or ear pathology * History of neurological disease (epilepsy, stroke, dementia, etc.) * Use of psychiatric medications (anxiolytics, antidepressants, antipsychotics, etc.) * Indications for emergency surgery * Planned spinal or epidural anesthesia * Conditions unsuitable for BIS monitoring * Cognitive impairment preventing informed consent

Design outcomes

Primary

MeasureTime frameDescription
Correlation between intraoperative noise levels and BIS values10-minute intervals intraoperative periodRelationship between mean intraoperative noise levels (LAeq, dB(A)) and mean Bispectral Index (BIS) values during the maintenance phase of general anesthesia.

Secondary

MeasureTime frameDescription
Relationship between intraoperative noise levels and hemodynamic parametersIntraoperative periodAssociation between average intraoperative noise level (LAeq, dB(A)) and hemodynamic variables (systolic blood pressure, diastolic blood pressure, mean arterial pressure, and heart rate). Hemodynamic parameters will be recorded at 5-minute intervals, while noise levels will be measured at 10-minute intervals.
Effect of noise source type on BIS and hemodynamic stabilityIntraoperative period.Evaluation of whether noise source categories (device-related, human-related, alarms, media) are associated with changes in BIS and hemodynamic parameters. Noise type will be recorded by independent observer every 10 minutes.
Comparison of BIS and hemodynamic outcomes across surgical branchesIntraoperative period.Surgical specialties will be classified into high, moderate, or low noise categories. BIS and hemodynamic data will be compared across these groups.

Contacts

CONTACTEmine Ozcan, MD
dr.emine3419@gmail.com+905301592856
PRINCIPAL_INVESTIGATOREmine Ozcan, MD

Başakşehir Çam & Sakura City Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026