Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07404956

THE EFFECT OF SURGICAL MASK AND N95 MASK USE ON SURGICAL SMOKE IN OPERATING ROOM NURSES

Led by Bartın Unıversity · Updated on 2026-02-12

38

Participants Needed

1

Research Sites

75 weeks

Total Duration

On this page

Sponsors

B

Bartın Unıversity

Lead Sponsor

B

Bartin State Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study was conducted to compare the effect of surgical mask and N95 mask use on physical symptoms due to surgical smoke in operating theatre nurses. The study, which was conducted in a single-group prospective quasi-experimental design, was completed with 38 nurses in the operating theatre unit of a state hospital in the Western Black Sea Region. Data were collected for four weeks using the Descriptive Information Form, Numerical Rating Scale and Symptom Follow-up Form. According to the findings, muscle weakness, myalgia in the upper extremities and muscle cramps were statistically significantly less in nurses using N95 masks. Respiratory parameters, watery eyes and redness were significantly lower in nurses using surgical masks. As a result, it was determined that the type of mask was effective on the incidence of physical symptoms related to surgical smoke.

CONDITIONS

Official Title

THE EFFECT OF SURGICAL MASK AND N95 MASK USE ON SURGICAL SMOKE IN OPERATING ROOM NURSES

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Willingness to participate in the study
  • Aged 18 years or older
  • Working as a sterile operating room nurse at least 4 hours per day, 5 days per week
  • Compliance with continuous use of both surgical mask and N95 mask for at least 4 hours per day
  • Ability to communicate verbally and provide informed consent
Not Eligible

You will not qualify if you...

  • Diagnosed psychiatric disorders
  • Presence of chronic respiratory, musculoskeletal, or neurological diseases
  • Presence of chronic dermatological conditions or allergies affecting the facial or respiratory area
  • Speech or communication impairments
  • Pregnancy
  • Holding a supervisory role or non-sterile nursing role
  • Planned unit change or rotation during the study period

AI-Screening

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Trial Site Locations

Total: 1 location

1

Bartın State Hospital

Bartın, Bartın, Turkey (Türkiye), 74100

Actively Recruiting

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Research Team

H

Hilal Çetin Baltutar, Nurse

CONTACT

S

Sevim Çelik, Proffessor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

2

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