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Reducing the Negative Effects of Surgical Conditions Use of Double Layer Mask Against Electrocautery With Smoke Filter

Not Applicable
Completed
Conditions
Surgical Procedure, Unspecified
Interventions
Device: smoke filtering electrocautery device
Other: double mask
Registration Number
NCT06550492
Lead Sponsor
Ataturk University
Brief Summary

This study was conducted to determine and compare the effectiveness of the smoke filtering electrocautery device used to reduce the negative effects of surgical smoke and the use of a double layer mask.

Detailed Description

The research was conducted as a randomised controlled experimental study. The research was collected between November 2023 and February 2024 in Atatürk University Health Research and Application Centre Operating Theatre unit. Data were collected using the Personal Information Form, Specified Health Problems Questionnaire, and the Practice Record Form to record blood gas laboratory results. The study was conducted with 90 (30 control, 30 double mask, 30 device) operating theatre workers. The population of the study consisted of Atatürk University Health Practice and Research Hospital Operating Theatre unit employees between November 2023 and February 2024. In this study, a priori power analysis was performed to determine the sample size. In the power analysis, the sample of the study consisted of a total of 90 people, 30 people in the group using cautery device with smoke filtering system, 30 people in the group using double masks and 30 people in the control group, with an effect size of 0.5%, which is the medium effect size according to Cohen, an error margin level of 0.05% and a confidence interval of 0.95%, with a 95% population representativeness.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
108
Inclusion Criteria
  • people over the age of 18.
  • People who agreed to participate in the study,
  • who have been working in the operating theatre for at least one year.
  • people who do not have chronic diseases Voluntary personnel who volunteered to co-operate were included in the study.
Exclusion Criteria
  • People who did not agree to participate in the study,
  • persons who have been working in the operating theatre for less than one year
  • people with chronic diseases,
  • people who withdrew from the study before all data were collected
  • Personnel whose laboratory results could not be analysed were excluded from the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
experimental group using smoke filtering electrocautery devicesmoke filtering electrocautery deviceexperimental group using smoke filtering electrocautery device
experimental group using double maskdouble maskexperimental group using double mask
Primary Outcome Measures
NameTimeMethod
Application Registration Form1 day

This form includes laboratory findings such as COHb, MetHb, PaO2, PaCO2, pH, HCO3, SpO2, Hg that may be affected in the person exposed to surgical smoke. In the study, it was examined whether exposure to surgical smoke affected these values.

Questionnaire on Reported Health Problems1-2 day

The questionnaire form, which was created by the researcher by reviewing the literature on the subject, includes 45 health problems that may occur in the short term as a result of exposure to surgical smoke and a scale related to the frequency of experiencing these problems. in the questionnaire, the every day option shows the maximum value, the never option shows the minimum value

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Atatürk University Health Application and Research Centre

🇹🇷

Erzurum, Yakutiye, Turkey

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