The study for the utility of Nasal High flow system during dental sedation in obesity patients with intellectual disability

The study for the utility of Nasal High flow system during dental sedation in obesity patients with intellectual disability - The utility of Nasal High flow system during dental sedation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000022499

Enrollment

Registered

2016-08-01

Start date

2017-01-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental diseases

Interventions

The use of Optiflow Oxygen administration by normal nasal cannula

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Being aged >= 16 years 2. Exhibiting an ASA physical state of 1 or 2 3. Body Mass Index (BMI) >= 25 4. Suffering from a severe intellectual disability and not cooperating fully with dental treatment

Exclusion criteria

Exclusion criteria: 1. Exhibiting an ASA physical state of >3 2. Being contraindicated for the use of midazolam or propofol.

Design outcomes

Primary

Measure	Time frame
1. Minimum arterial oxygen saturation (SAT) during sedation.	—

Secondary

Measure	Time frame
1. The frequency and duration of SAT<=94% during sedation. 2. The frequency and duration of SAT<=90% during sedation. 3. Arterial oxygen pressure and arterial carbon dioxide pressure 4. Assisted ventilation with a bag valve mask	—

Countries

Japan

Contacts

Public ContactHitoshi Hitoshi

Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Department of Dental Anesthesiology and Special Care Dentistry

higuti@md.okayama-u.ac.jp086-235-6721

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026