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Self-retaining Bicanalicular Intubation Stent Versus Bicanalicular Silicone Tube for Management of Canalicular Obstruction

NCT04706117 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2021-02-24

No results posted yet for this study

Summary

The aim of the study is to evaluate outcomes of the use of self\_retaining intubation set versus bicanalicular silicone tube in management of canalicular obstruction

Conditions

  • Canalicular Obstruction

Interventions

DEVICE

Self-retaining bicanalicular intubation stent

self-retaining bicanaliculs intubation setII(SRSII) which is the latest innovation in the field as these silicone stent segments traverse both canaliculi till the lacrimal sac. In which each end of this semicircular device has 2 stout angulated wings/flanges which pose no resistance while proceeding forward into the canaliculus, but once they get into open cavity (lacrimal sac), the flanges open up and give resistance to their removal against the common canalicular opening

Sponsors & Collaborators

  • Minia University

    lead OTHER

Principal Investigators

  • Ahmed M Elshafei · Minia University

  • Raafat M Abdelrahman · Minia University

  • Amr A Mohrmed, I · Minia University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-02-28
Primary Completion
2021-06-30
Completion
2021-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04706117 on ClinicalTrials.gov