Evaluating aerosol management in dental clinics during Covid-19
Evaluation of Aerosol in a Dental Clinic
PHASE4 · The University of Texas Health Science Center, Houston · NCT04659928
This study tests different methods to reduce the risk of Covid-19 for dental workers during procedures that create aerosols, like using special vacuum devices and mouth rinses.
Quick facts
| Phase | PHASE4 |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | The University of Texas Health Science Center, Houston (other) |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT04659928 on ClinicalTrials.gov |
What this trial studies
This study assesses the effectiveness of various external evacuation units and mouth rinses during aerosol-generating procedures in dental clinics. It aims to determine the risk level to dental practitioners when performing these procedures in the context of Covid-19. The interventions include high volume evacuation, extraoral vacuum aspirators, external evacuation devices, and hydrogen peroxide as a mouth rinse. The study will focus on procedures that involve prepping natural teeth and are scheduled for the first appointment of the day.
Who should consider this trial
Good fit: Ideal candidates for this study are patients requiring dental procedures that involve prepping natural teeth and can accommodate a longer appointment time.
Not a fit: Patients who do not require dental procedures or those with shorter appointment times may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance safety protocols for dental practitioners and reduce the risk of Covid-19 transmission during dental procedures.
How similar studies have performed: Other studies have explored aerosol management in healthcare settings, but this specific approach in dental clinics is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * prepping natural teeth at the appointment * at least an hour long procedure * procedure will be the first one in the morning
Where this trial is running
Houston, Texas
- The University of Texas Health Science Center at Houston — Houston, Texas, United States (RECRUITING)
Study contacts
- Principal investigator: Claudia Ruiz Brisuela, DDS — The University of Texas Health Science Center, Houston
- Study coordinator: Claudia Ruiz Brisuela, DDS
- Email: Claudia.RuizBrisuela@uth.tmc.edu
- Phone: (713) 486-4138
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Covid19