Clinical Trials Directory

Trials / Unknown

UnknownNCT04148170

Recanalization of Congenital Nasolacrimal Duct Obstruction by Endodiathermy Probe and Intubation Versus Intubation Only

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
2 Years – 7 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

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

Conditions

Interventions

TypeNameDescription
PROCEDUREEndodiathermy Probe and Intubation Versus Intubationchildren suffer from congenital nasolacrimal duct obstruction will have probing with endodiathermy probe and then intubation with bicanlicular silicon tube

Timeline

Start date
2020-03-01
Primary completion
2020-06-01
Completion
2020-09-01
First posted
2019-11-01
Last updated
2019-11-01

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04148170. Inclusion in this directory is not an endorsement.