The safety and efficacy of silicone tube for the management of watering eye
Phase 4
- Registration Number
- CTRI/2009/091/000923
- Lead Sponsor
- Aurolab
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects having epiphora
Canalicular blockade ascertained with probing
Chronic dacryocystitis
Mucocele
Exclusion Criteria
Absent puncta
Acute on chronic dacryocrystitis
Noticeable lid laxity
Previous lacrimal surgery
Patients younger than 15 years
Suspicion of malignancy
Post traumatic lids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Resolution of epiphoraTimepoint: 15th day, 1st month, 6th month, and 12th month.
- Secondary Outcome Measures
Name Time Method Post operative complicationsTimepoint: 15th day, 1st month, 6th month and 12th month