The Safety and Efficacy of Lacrimal Silicone Intubation for the Management of Epiphora
NCT01010659 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2011-07-15
Summary
The purpose of study is to investigate the safety and efficacy of lacrimal silicone intubation for the management of epiphora.
Conditions
- Epiphora
Interventions
- DEVICE
-
Lacrimal Tube
Lacrimal Tube
Sponsors & Collaborators
-
Aurolab
lead OTHER
Principal Investigators
-
Dr. Usha Kim, MBBS, DO · Aravind Eye Hospital
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 15 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-11-30
- Primary Completion
- 2011-03-31
- Completion
- 2011-06-30
Countries
- India
Study Locations
More Related Trials
-
Six Month Study to Evaluate the Safety and Effectiveness of the Intranasal Lacrimal Neurostimulator
NCT02526290 ·Status: COMPLETED ·Phase: NA
-
Pilot Study to Clinical Evaluate Device Prototypes in Dry Eye Patients
NCT01957670 ·Status: WITHDRAWN ·Phase: NA
-
Evaluating a Device for Blocking the Tear Duct
NCT05748951 ·Status: COMPLETED ·Phase: NA
-
Effect of Chitosan-N-acetylcysteine on Subjective Pain Sensation in Corneal Abrasion
NCT05049642 ·Status: TERMINATED ·Phase: NA
-
Efficacy of Topical Cyclosporine Versus Tears for Improving Visual Outcomes Following Multifocal IOL Implantation
NCT00349583 ·Status: COMPLETED ·Phase: PHASE4
-
Multicenter Trial Evaluating Quality of Tears Produced by Nasal Neurostimulation
NCT02385292 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Cyclosporine Ophthalmic Emulsion in the Treatment of Dry Eye Syndrome in Contact Lens Wearers
NCT00335114 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Different Treatment Regimens With Chitosan-N- Acetylcysteine in Moderate-to-severe Dry Eye Disease
NCT05053789 ·Status: TERMINATED ·Phase: NA
-
Study to Evaluate Corneal Neurosensory Abnormalities in Patients With Sjögren's Dry Eye
NCT06411132 ·Status: TERMINATED
-
Efficacy Study of Cyclosporine Ophthalmic Emulsion in Patients With Dry Eye Disease
NCT00717418 ·Status: COMPLETED
-
Goblet Cell Degranulation Produced by Intranasal Tear Neurostimulator (ITN) in Dry Eye Disease
NCT03827564 ·Status: TERMINATED ·Phase: NA
-
Use of Autologous Serum Eye-drops as Tears in Patients With Recalcitrant Dry Eye
NCT01089985 ·Status: COMPLETED ·Phase: PHASE1
-
Does the Use of a Moisture Chamber Decrease the Incidence of Corneal Abrasions in Critically Ill Pediatric Patients?
NCT00129077 ·Status: COMPLETED ·Phase: NA
-
Treatment of Dry Eye Syndrome With Cyclosporin A Eye Drops
NCT00001731 ·Status: COMPLETED ·Phase: PHASE2
-
Comparing the Quality of Topical Autologous Serum in Different Etiologies of Dry Eye Syndrome
NCT02774707 ·Status: UNKNOWN
-
Tear Film Markers in Dry Eye Syndrome
NCT04515329 ·Status: WITHDRAWN ·Phase: PHASE4
-
To Evaluate the Efficacy and Safety of LO2A Eye Drops in Patients With Conjunctivochalasis
NCT02810119 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects
NCT01010282 ·Status: COMPLETED ·Phase: NA
-
Determination of the Optimum Delivery Route for Botulinum Toxin A in Patients With Epiphora
NCT01282541 ·Status: COMPLETED ·Phase: PHASE2
-
Study for Remote Investigation of Evaporative Dry Eye Disease
NCT06976515 ·Status: RECRUITING
-
Study on Safety and Performance of an Artificial Tear in Dry Eye Treatment in Subjects With Ocular Surface Inflammation
NCT04633863 ·Status: COMPLETED ·Phase: NA
-
Topical Tacrolimus 0.03% Ointment for Intractable Allergic Conjunctivitis: An Open Label Pilot Study
NCT00443105 ·Status: UNKNOWN ·Phase: PHASE2
-
A Study to Assess the Safety and Efficacy of IC265 Ophthalmic Solution for Dry Eye in Adult Participants
NCT05992922 ·Status: TERMINATED ·Phase: PHASE2
-
A Novel Combined Therapy for Refractory Vernal Keratoconjunctivitis
NCT03464435 ·Status: COMPLETED ·Phase: PHASE4
-
Study of the TearCare System in Dry Eye Disease
NCT03588624 ·Status: COMPLETED ·Phase: NA