Smoke Clinical Trial
Official title:
The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aerosols in Operating Rooms at a University Hospital, Thailand
This study aims to evaluate the pre-post smoke evacuation uses on surgical smoke and bio-aerosols particles in operating rooms at a university hospital, Thailand.
Purpose of Project
Smoke and bio-aerosols are routinely produced by surgical instruments; eg, lasers,
electrosurgical units, radiofrequency devices, ultrasonic devices, power tools. Plume and
bio-aerosols contain odor-causing and odorless toxic gases, vapors, dead and live cellular
debris (including blood fragments), and viruses. These airborne contaminants can pose
respiratory, ocular, dermatological and other health-related risks, including mutagenic and
carcinogenic potential, to patients and operating room personnel. The National Institute of
Occupational Safety and Health (NIOSH) and the Center for Disease Control (CDC) have also
studied electrosurgical smoke at length. Therefore, the equipment of smoke evacuation in OR
needs to be used. Therefore, this study aims to evaluate the pre-post smoke evacuation uses
on surgical smoke and bio-aerosols particles in operating rooms at a university hospital,
Thailand.
Methodology Association of periOperative Registered Nurses (AORN) guideline is used as the
conceptual framework of this study including evidence based practice for smoke and
bio-aerosols evacuation systems. The study design is a quasi-experimental study
(manipulation and control only, without randomization) comparing the amount of surgical
smoke and bio-aerosols particles pre- post smoke evacuation uses. The samples consist of 64
cases of surgical patients who receive head-neck or breast surgery and 64 cases of surgical
patients who receive abdominal laparoscopic surgery. The amount of surgical smoke and
bio-aerosols' particles in the surgical field and OR environment are measured by AeroTraxTM
Handheld Airborne Particle Counter Model 9306.
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Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
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Not yet recruiting |
NCT05367219 -
Smoke of Endoscopic Gastrointestinal Surgery
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N/A |