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To study the use and side effects of Netarsudil 0.02 percent eye drops in patients of glaucoma.

TO STUDY THE EFFICACY AND SAFETY OF NETARSUDIL OPHTHALMIC SOLUTION 0.02 PERCENT IN PATIENTS OF POAG. - nil

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/068149
Enrollment
130
Registered
2024-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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: Netarsudil plus Timolol: Netarsudil 0.02 percent administered topically to eye once daily in night for three month and Timolol 0.5 percent used in eye topically twice daily for three mo

Sponsors

Northern Railway Central Hospital Basant Lane Aram Bag Paharganj New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Already diagnosed case of POAG on one of the standard drug that will be Timolol 0.5 percent eye drop for more than 1month. 2. Age at least 45 years and above. 3 .IOP more than 17mmhg and less than 25 mmhg. 4. BCVA 6/9 or better by Snellens chart.

Exclusion criteria

Exclusion criteria: Any ocular disease likely to affect IOP. Any pathology of eye affecting media clarity. Any infective /inflammatory pathology of eye at screening time. Any ocular trauma in last 6 month . CCT OF patients more than 625 micron. Hypertension. Advanced changes of glaucomatous optic nerve.

Design outcomes

Primary

MeasureTime frame
To compare the IOP reduction between the combination therapy of netarsudil with timolol versus timolol monotherapy calculated by averaging the mean IOP over a period of 3 month. Timepoint: 3 month

Secondary

MeasureTime frame
The ocular safety variables with netarsudil are ocular symptoms like dry eyes, ,corneal deposits, corneal verticillata ,conjunctival hemorrhage ,corneal staining ,headaches, blurry vision,instillation site pain, erythema.Timepoint: 3 month

Countries

India

Contacts

Public ContactShailender Kumar Choudhary

Norhtern Railway Central Hospital

shailenderchoudhary@rediffmail.com9717630563

Outcome results

None listed

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