Study on awaking from intravenous sedation -Analysis Using Wearable Type of Eye Movement Measuring Apparatus TalkEye Lite-

Study on awaking from intravenous sedation -Analysis Using Wearable Type of Eye Movement Measuring Apparatus TalkEye Lite- - Study on awaking from intravenous sedation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000014144

Enrollment

Registered

2014-06-20

Start date

2014-06-20

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

Healthy adults

Interventions

Intravenous sedation involved a single administration of 0.05mg/kg midazolam

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The healty adult male and female volunteers participated this study. We obtained informed concent from all subjects

Exclusion criteria

Exclusion criteria: Patient of two degree or more of ASAclassification Age of under 20 Have a drug Allergy

Design outcomes

Primary

Measure	Time frame
1.Eye movement 2.Romberg's test 3.Electroencephalogram 4.Clinical presentation 5.Sedation score 6.Vital sign	—

Countries

Japan

Contacts

Public ContactYuya Tomita

The Nippon Dental University School of Life Dentistry at Niigata Department of Dental Anesthesiology

ytomita@ngt.ndu.ac.jp0252671500

Outcome results

None listed

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