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Feasibility of monitoring depth of analgesia by ultrasound of pupillary dilated reflex diameter in response to nociceptive stimulation

Feasibility of monitoring depth of analgesia by ultrasound of pupillary dilated reflex diameter in response to nociceptive stimulation - Feasibility of monitoring depth of analgesia by ultrasound of pupillary dilated reflex diameter in response to nociceptive stimulation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000047145
Enrollment
15
Registered
2022-03-11
Start date
2020-01-01
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

Adult healthy volunteers

Interventions

None listed

Sponsors

Hirosaki University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy adults.

Exclusion criteria

Exclusion criteria: Any ocular disease , neurological diseases , history of any type of ocular surgery or laser treatment and taking topical or systemic medications potentially affecting pupillary function.

Design outcomes

Primary

MeasureTime frame
Pupil dilation reflex change in response to noxious stimulation measured by infrared video pupillometry and ultrasonography.

Secondary

MeasureTime frame
NRS(Numerical Rating Scale) after noxious stimulation.

Countries

Japan

Contacts

Public ContactMao Konno

Hirosaki University Hospital Anesthesiology

mao511@hirosaki-u.ac.jp0172-33-5111

Outcome results

None listed

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