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checking the efficacy of triple fixed dose combination-timolol, brinzolamide and brimonidine in patients with open angle glaucoma and ocular hypertension not responding to dual drug therapy

Novel triple fixed dose combination- timolol,brinzolamide and brimonidine in patients with open angle glaucoma and ocular hypertension not responding to dual drug therapy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067045
Enrollment
60
Registered
2024-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H401- Open-angle glaucoma

Interventions

Intervention1: NIL: NIL

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients of either gender aged more than 18 years, baseline IOP more than18mmHg ,with a diagnosis in each eye of either: 2) Ocular hypertension 3) Chronic or primary open angle glaucoma 4) Chronic angle closure glaucoma with patent PI 5) Pseudoexfoliative glaucoma 6) Pigmentary glaucoma

Exclusion criteria

Exclusion criteria: 1) Known allergy, contraindication, hypersensitivity, or contraindication to the study medication or any of its components 2) active ocular disease other than glaucoma or OHT (except chronic mild blepharitis, cataract, age-related macular degeneration, or background diabetic retinopathy, which could be enrolled at the discretion of the investigator) 3) recent or anticipated changes in therapy for chronic conditions with agents that could affect IOP 4) corneal abnormalities that could preclude accurate IOP readings with applanation tonometry 5)use of corticosteroids within defined exclusion periods prior to baseline and through the study period 6) incisional surgery or laser procedure within defined exclusion periods prior to baseline

Design outcomes

Primary

MeasureTime frame
checking intraocular pressure on DAY 0, 2nd week, 6th week, 12th weekTimepoint: checking intraocular pressure on DAY 0, 2nd week, 6th week, 12th week

Secondary

MeasureTime frame
to check the efficacy and safety of the triple fixed dose combinationTimepoint: to check the efficacy and safety of the triple fixed dose combination

Countries

India

Contacts

Public ContactDR SHIBI DEV BN

Nethradhama superspeciality eye hospital

drshibidev@gmail.com9986777892

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026