Efficacy of the respiratory sound monitoring system during dental sedation

JRCT ID: jRCTs062220054

Registered date:31/08/2022

Basic Information

• Recruitment status: Complete
• Health condition(s) or Problem(s) studied: Indications for dental treatment
• Date of first enrollment: 22/09/2022
• Target sample size: 60
• Study type: Interventional
• Intervention(s): Conduct respiratory sound sampling with some water in the mouth.

Outcome(s)

• Primary Outcome: Abnormal Respiration INDEX

Secondary Outcome

1) Respiratory discrimination performance
2) Interview from anesthesiologist

Key inclusion & exclusion criteria

• Age minimum: >= 18age old
• Age maximum: Not applicable
• Gender: Both
• Include criteria: Patients with sedation during dental treatment.

Exclude criteria

1. Patients has an allergic to midazolam or propofol.
2. Patients with a history of serious adverse reactions to midazolam or propofol in the past.
3. Patients with dysphagia.
4. Patients with poor oral hygiene
5. Patients with mentally retarded.
6. Minor patients.
7. Patients whom the investigator deems appropriate to be excluded from the study.

Related Information

• Primary Sponsor: Shimizu Yoshitaka