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Measurement of damage with dacryoendoscopic examination and treatment

Measurement of physical distress with dacryoendoscopic examination and treatment - Physical distress with dacryoendoscopic examination and treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000040710
Enrollment
200
Registered
2020-06-10
Start date
2017-09-01
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

lacrimation and epiphora

Interventions

None listed

Sponsors

Ehime University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with lacrimation or epiphora Patients with lacrimal duct obstruction who were treated with dacryoendoscopic probing and intubation

Exclusion criteria

Exclusion criteria: a) Patients who do not agree with this survey b) Patients who are judged to be unsuitable for participation in this study by the investigator

Design outcomes

Primary

MeasureTime frame
1, Assessment of distress scale of each step in dacryoendoscopic examination 2, 1, Assessment of distress scale of each step in dacryoendoscopic probing and intubation

Secondary

MeasureTime frame
1, Comparison of distress scale of dacryoendoscopic examination between pre and post operation 2, Comparison of distress scale of dacryoendoscopic probing and intubation between canalicular and nasolacrimal duct obstruction 3, Development of anesthesia to reduce physical distress

Countries

Japan

Contacts

Public ContactTomoyuki Kamao

Ehime University Ophthalmology

t-kamao@m.ehime-u.ac.jp+81-89-960-5361

Outcome results

None listed

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