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The Factors That Affected the Outcome of Treatment of Congenital Nasolacrimal Duct Obstruction

Completed
Conditions
Congenital Nasolacrimal Duct Obstruction
Interventions
Procedure: Probing
Registration Number
NCT02081781
Lead Sponsor
Cathay General Hospital
Brief Summary

The purpose of this study was to investigate various potential factors that affected the outcome of treatment of congenital nasolacrimal duct obstruction.

Detailed Description

Congenital nasolacrimal duct obstruction is a common condition during the first few years of childhood. Most cases may resolve spontaneously, but the remaining children whose blockage does not resolve may require primary probing. Controversy remains regarding the optimal timing of the probing procedure. Another controversy is related to the setting of surgery. Therefore, we try to investigate the factors that affected the outcome of treatment of congenital nasolacrimal duct obstruction under the same surgical doctor during the past 13 years in our hospital.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
800
Inclusion Criteria
  • a history of tearing and/or mucopurulent discharge beginning during the first few weeks of life
  • anatomical nasolacrimal duct obstruction
Exclusion Criteria
  • previous probing
  • glaucoma
  • trauma
  • lid malpositions
  • craniofacial anomalies
  • congenital mucocele of the nasolacrimal sac

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Probing, topical anesthesiaProbingNasolacrimal duct obstruction (NLDO) is a quite common condition among the infants. An imperforate membrane at the distal end of the nasolacrimal duct is the main cause of occlusion. Children with the signs of NLDO presenting with epiphora and/or mucous discharge were included in this study. Intervention with probing under topical anesthesia was performed on the same surgeon. And success rate was evaluated.
Primary Outcome Measures
NameTimeMethod
probing success: both anatomical patency of the duct and functional free of symptomsone week
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Ophthalmology, Cathay General Hospital

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Taipei, Taiwan

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