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Development of a robotic sedation system

Clinical trials for the development of a robotic sedation system

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1022250006
Enrollment
60
Registered
2025-06-04
Start date
2025-07-01
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

Patients undergoing dental or oral surgery Dental treatment, oral surgery

Interventions

Sponsors

Hoshijima Hiroshi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients undergoing surgery under intravenous sedation at the Department of Dentistry and Oral Surgery, Tohoku University Hospital

Exclusion criteria

Exclusion criteria: (1) People with poor overall health (heart disease, lung disease, high blood pressure, diabetes, etc.) (2) Patients with allergies to eggs or soybeans (3) Women who are pregnant, may be pregnant, within 28 days of giving birth, or breastfeeding (4) Patients with psychiatric illness or symptoms that make it difficult for them to participate in the study (5) Children

Design outcomes

Primary

MeasureTime frame
Estimated Dosage of Propofol

Secondary

MeasureTime frame
The type and frequency of system malfunctions

Contacts

Public ContactHiroshi Hoshijima

Tohoku University Graduate School of Dentistry

hhoshi6@gmail.com+81-22-717-8420

Outcome results

None listed

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