Congenital Nasolacrimal Duct Obstruction Clinical Trial
Official title:
Recanalization of Congenital Nasolacrimal Duct Obstruction by Endodiathermy Probe and Intubation Versus Intubation Only
The purpose of the current work is to assess the efficiency and success rate of endodiathermy probe followed by intubation in children more than 2 years compared to the success rate of intubation (as a standard method) which varies from 75% to 85% in several studies
The study will be conducted on children above 2 year and will be divided randomly into two
groups:
Group (I): 80 eyes of children suffer from congenital nasolacrimal duct obstruction will have
probing with metal probe and then intubation with bicanlicular silicon tube.
Group (II): 80 eyes of children suffer from congenital nasolacrimal duct obstruction will
have probing with endodiathermy probe and then intubation with bicanlicular silicon tube
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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Safety and Efficacy Study of Besivance™ for Treatment of Congenital Nasolacrimal Duct Obstruction in Children
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Endoscopy Assisted Probing Versus Simple Probing in Primary Congenital Nasolacrimal Duct Obstruction
|
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| Completed |
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The Factors That Affected the Outcome of Treatment of Congenital Nasolacrimal Duct Obstruction
|
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