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lacrimal endoscopy study

Comparison of dacryocystography and lacrimal endoscopy in patients with epiphora - prospective clinical research

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002578
Enrollment
37
Registered
2017-12-01
Start date
2017-06-27
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Medical Device : Dacryocystography and lacrimal endoscopy were performed and clinical results were compared.

Sponsors

Chung-Ang Univerisity Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? men or women with ages of over 19 ? patients with symptoms of tearing, increased tear meniscus height, and positive for dye disappearance test ? patients with partial or complete lacrimal pathway obstruction confirmed by lacrimal irrigation ? Those who have read and agreed to the informed consent from prior to carrying out the research

Exclusion criteria

Exclusion criteria: ? pregnant or lactating women ? Thoes who can not rea the written consent(illiterate, foreigner) ? patients with allergic to contrast media

Design outcomes

Primary

MeasureTime frame
diagnostic consistency between dacryocystography and lacrimal endoscopy

Secondary

MeasureTime frame
sensitivity and specificity of dacryocystography and lacrimal endoscopy

Countries

Korea, Republic of

Contacts

Public ContactJeong Kyu Lee

Chung-Ang Univerisity Hospital

lk1246@hanmail.net+82-2-6299-1688

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026