Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07404956

Comparison of Effects of Surgical Mask and N95 Mask Use on Physical Symptoms Caused by Surgical Smoke in Operating Room Nurses

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

38

Participants Needed

1

Research Sites

23 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

Researchers are evaluating the effects of using surgical masks compared to N95 masks on physical symptoms caused by surgical smoke in operating room nurses. The study focuses on understanding how different types of masks impact symptoms such as muscle weakness, respiratory issues, and eye irritation related to exposure to surgical smoke during surgeries. This interventional study involves nurses working in a hospital operating theatre setting. The study includes two groups where operating room nurses wear either a standard surgical mask or an N95 respirator during surgical procedures with exposure to surgical smoke. The nurses use each type of mask continuously for at least four hours per day over a four-week period. Physical symptoms are monitored and compared between the two mask types to assess their effect on symptom severity. Participants are asked to use the assigned mask type during surgeries and report their symptoms daily using rating scales and symptom tracking forms. Data collection occurs five days a week for four weeks both before and after surgery. Researchers measure physical symptoms such as muscle weakness, myalgia, muscle cramps, respiratory parameters, watery eyes, and redness. The study monitors symptom severity using a numerical rating scale and evaluates the differences between mask types to understand the impact on surgical smoke-related symptoms.

CONDITIONS

Brief 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
  • Willingness and ability to continuously wear 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
  • Chronic respiratory, musculoskeletal, or neurological diseases
  • Chronic dermatological conditions or allergies affecting the face or respiratory area
  • Speech or communication impairments
  • Pregnancy
  • Holding a supervisory or non-sterile nursing role
  • Planned unit change or rotation during the study period

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - 4 weeks

Participants wear surgical masks and N95 respirators during surgical procedures with exposure to surgical smoke to compare physical symptoms caused by the smoke.

Five days per week

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

S

Sevim Çelik, Proffessor

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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