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N/A N=50 Randomized Prevention

Reducing Aerosol and Bioaerosol Using Different Oral Suctions

Infections · Oral Infection

Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Apr 2025
Primary outcome: Primary: Particulate Matter (PM) — 121.3; 135.1; 147.6; 128.4 micrograms per cubic meter (µg/m³)

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
low suction (Device); intraoral suction (Device); high & low suction (Device); extra-oral suction & low suction (Device); Extra-Oral Suction and Intraoral Suction (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
King Abdulaziz University
Primary completion
Sep 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Particulate Matter (PM)
121.3; 135.1; 147.6; 128.4; 136.9
PRIMARY
Microbial Count
1117; 325.1; 100.2; 74.2; 45.6

Summary

Aerosol particles generated when using dental instrument such as ultrasonic and high air driven handpieces, this aerosol is mixture of blood, saliva, infectious agents, and dental materials. Inhaler dust that range between PM2.5 to PM10 could transferred to the human lung's terminal bronchioles and alveoli that cause a harm effect. The aim of this study to assess the effectiveness of different dental suction devices that could be contributed to decrease risk of particles count, Bacterial and fungal that arising from patient mouth to indoor air dental clinic. This is a randomized clinical trial will be conducted in three different places: educational hospital, public hospital, and private clinic. In each place 40 subject will be recruited. Measurement including particles count and microorganism will be taken before 15 minutes and during of scaling and prophylaxis procedure to measure particles count, oral bacteria, fungus, and microbial air. In this study will be compared between four intervention groups; Group A with high and low suction only, Group B using dry shield suction and low section, Group C using extra-oral suction with high and low suction, and Group D using dry shield suction and extra-oral suction and low section. Difference between each categorical groups and particle, oral bacterial, fungus, and microbial air concentration will be tested using two-way ANOVA test or one way ANOVA test. Statistical analysis will be carried using STATA version 13.

Eligibility Criteria

Inclusion criteria

  • Adult healthy patient above 18 years of age
  • Has scheduled an appointment at dental hygienist clinic for scaling procedure.
  • Has at least one score 2 or 3 in one sextant according to community periodontal index of treatment needs (CPITN).

Exclusion criteria

  • Number of teeth less than 20 teeth
  • Presence of soft or hard tissue lesions
  • Pregnant women
  • Orthodontic patient
  • Partial denture wearer
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05848245). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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