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Evaluation of success rate of primary monocanalicular intubation for Congenital Nasolacrimal Duct Obstruction in the cases of difficult irrigation

Evaluation of success rate of primary monocanalicular intubation for Congenital Nasolacrimal Duct Obstruction in the cases of difficult irrigation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201208074580N3
Enrollment
70
Registered
2014-07-22
Start date
2013-06-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Congenital Nasolacrimal Duct Obstruction. congenital stenosis and stricture of lacrimal duct

Interventions

All children will undergo probing of lacrimal duct, under general anesthesia, by an oculoplastic fellowship surgeon through upper canalicule with probe(00).Then lacrimal duct irrigation will be per
Treatment - Surgery

Sponsors

Vice-chancellor for Research and Technology of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Months to 1 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria;1- Age: 12-23 months of age 2- Chief complaint: epiphora and discharge since born 3-Difficult irrigation during probing 4-Informed consent of parents . Exclusion criteria: 1– Previous lacrimal duct of tear duct surgery or nasolacrimal duct intubation 2- Presence of Down syndrome 3- Proximal part of lacrimal system anomalies such as punctual agenesis 4 - History of lacrimal duct system trauma 5- Craniofacial anomalies 6 – Follow up less than 6 months after surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Epiphora or purulent discharge. Timepoint: 1 week,1 month, 3 month, 6 month after surgery. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Side effects such as complications like panctum changes and corneal complications include abration and early exit stent in all children. Timepoint: 1 week, 1 month, 3 month, and 6 month after surgery. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Dima Andalib

Tabriz University of Medical Sciences

dima1366@yahoo.com+98 41 1335 7310

Outcome results

None listed

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