The Effect of Masks on Surgical Smoke Exposure

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorMersin University

About this trial

Surgical smoke refers to the gaseous plume released into the air as a result of the thermal destruction of tissues by energy-based devices used in operating rooms. The composition of surgical smoke may include various organic compounds. In the literature, the most frequently identified chemical substances in surgical smoke are formaldehyde, acrolein, hydrocarbons, fatty acids, hydrocyanic acid, phenols, nitriles, acrylonitrile, hydrogen cyanide, benzene, and toluene. These particles can negatively affect the health of the operating room personnel. According to current guidelines, masks are recommended as the primary personal protective equipment to prevent respiratory exposure associated with surgical smoke. During surgical procedures, operating room staff frequently use surgical masks. Although surgical masks are the most commonly preferred personal protective equipment to protect healthcare workers against microorganisms and aerosols, they are unfortunately ineffective in filtering small particles. Therefore, the present study aimed to determine the impact of different types of masks on exposure to surgical smoke.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Use of electrocautery,

Duration of surgery longer than 2 hours,

Elective total or partial hip prosthesis procedures.

Disqualifiers

No use of electrocautery,

Duration of surgery shorter than 2 hours,

Emergency total or partial hip prosthesis procedures.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Particle counter

    Device

    The collection of air samples will begin with the surgical incision and will continue for 10 minute

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Single surgical maskExperimental treatment 1 intervention
Group B: Double surgical maskExperimental treatment 1 intervention
Group C: N95 maskExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in airborne particle count

Difference in particle count between masks

Time frame
The number of particles in the air collected during the 10 minutes following the initiation of the surgical incision.

Secondary outcomes

Other outcomes

Sponsors and contacts

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