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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05636488
Other study ID # 2022-07/1932
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date December 1, 2022
Est. completion date December 1, 2023

Study information

Verified date November 2022
Source Baskent University
Contact Begüm Ne Gökdemir
Phone +905389598290
Email begokdemir@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to learn about effects of noise in healthy patients undergoing elective surgery.


Description:

There are many factors that can negatively affect surgical performance in operating rooms. Noise is the most striking of these factors. Excessive noise can cause hearing loss, cognitive dysfunction, anxiety, stress-induced increases in cortisol levels, and an increased risk of cardiovascular disease. Noise can have negative effects on concentration and performance. At the same time, workplace noise is one of the most important causes of fatigue. One of the anesthesia phases where the sound level reaches the highest levels is the induction phase. With this study, the investigators want to examine the effects on the anesthesia team, the patient and the environment by measuring the noise levels during the induction period, and then train the operating room personnel to examine the effects on this issue. The investigators aim to raise awareness about the development of procedures and training programs for operating room personnel.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 500
Est. completion date December 1, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients over the age of 18, - Elective cases to be taken under general anesthesia, - Those who do not have a psychiatric disease, - Patients without hearing loss Exclusion Criteria: - patients under the age of 18 - Patients who have psychiatric disease - Patients who has hearing loss

Study Design


Intervention

Other:
No intervention
There is no intervention group in this study

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Baskent University

Outcome

Type Measure Description Time frame Safety issue
Primary assessing effect of noise level on fatigue with questionnaire A quieter environment can be created if noise level can be shown to cause fatigue in work performance. postoperative 24 hours
Primary assessing effect of noise level on anxiety with questionnaire A quieter environment can be created if noise level can be shown to cause anxiety in work performance. postoperative 24 hours
See also
  Status Clinical Trial Phase
Completed NCT04601909 - FX-322 in Adults With Age-Related Sensorineural Hearing Loss Phase 1
Not yet recruiting NCT05511753 - The Effect of Acupuncture on Patients With Noise-induced Hearing Loss N/A
Completed NCT04120116 - FX-322 in Adults With Stable Sensorineural Hearing Loss Phase 2
Completed NCT05086276 - FX-322 in Adults With Acquired Sensorineural Hearing Loss Phase 2
Not yet recruiting NCT02779192 - A Phase 2b Study of SPI-1005 to Prevent Acute Noise Induced Hearing Loss Phase 2
Completed NCT04629664 - FX-322 in Adults With Severe Sensorineural Hearing Loss Phase 1
Enrolling by invitation NCT04183361 - ABR Characteristics and Salivary Cortisone Concentration in Noise-exposed Workers