Health Condition 1: H401- Open-angle glaucoma
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Newly diagnosed glaucoma patients started on topical preservative free travoprost monotherapy (0.004%) 2. Patients having diameter of punctum >=0.3 mm(0.3-0.5 mm) on slit lamp biomicroscopy before starting travoprost. 3. Patients having pretreatment imaging parameters of proximal lacrimal drainage system within normal range as measured by ASOCT.
Exclusion criteria
Exclusion criteria: 1. Patients diagnosed with glaucoma and started on treatment earlier. 2. History of long term ( more than 2 weeks) use of topical medications and oral medications likely to alter LDS. 3. Patient requiring adjuvant treatment to lower IOP during the study. 4 pretreatment abnormal imaging parameters of PLDS recorded by ASOCT. 5. Diseases of LDS like punctal and canalicular stenosis, atresia, agenesis, canaliculitis, nasolacrimal duct Obstruction NLDO, tumours/ lesions involving the LDS. 6. Eyelid malpositions like ectropion, entropion. 7. Cicatrising ocular diseases likely to affect LDS like Steven Johnson Syndrome, Ocular cicatricial pemphigoid, chronic conjunctivitis etc. 8. Any previous history of surgeries on LDS, eyelid. 9. History of ocular trauma involving the eyelids, LDS. 10. Previous history of ocular radiotherapy for various causes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study the effect of preservative free travoprost on proximal lacrimal drainage system in newly diagnosed glaucoma patients using ASOCT.Timepoint: At presentation (baseline), and on follow up visit at 3rd, 6th, 9th and 12th month. | — |
Secondary
| Measure | Time frame |
|---|---|
| Measurement of external punctal diameter, internal punctal diameter and vertical canalicular depth on ASOCT..Timepoint: At presentation (baseline), and on follow up visit at 3rd, 6th, 9th and 12th month. | — |
Countries
India
Contacts
Sankara eye hospital, Shimoga.