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To check efficacy of ripasudil in management of primary open angle glaucoma

Efficacy and Safety of Ripasudil in the Treatment of Primary open angle glaucoma and Ocular Hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033754
Enrollment
60
Registered
2021-05-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: 4- Measurement and Monitoring Health Condition 2: H401- Open-angle glaucoma

Interventions

Intervention1: Ripasudil : eye drop Ripasudil hydrochloride 0.4% dose : Twice daily for 3 months Control Intervention1: Eye drop Timolol: eye drop timolol 0.5% dose: twice daily for 3 months

Sponsors

Dr Sowparnika A B
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Newly detected POAG / OHT. 2. POAG will be defined as: a. IOP > 21 mmHg on atleast 2 occasions, atleast 24 has apart. b. Optic nerve head showing CDR > 0.61 with significant thinning of the neuroretinal rim: or a CDR asymmetry of 0.2 > between 2 eyes. c. Open angles on gonioscopy. d. Automated visual field testing showing changes corresponding with the optic disc changes. 3. OHT will be defined as: • IOP > 21 mmHg on atleast 2 occasions, 24 hrs apart. • Open angles on gonioscopy • Normal optic disc and visual field tests 4. Patients willing to participate in the study given a written informed consent and comply with the followup schedule.

Exclusion criteria

Exclusion criteria: 1. Patients with POAG / OHT having IOP > 30 mmHg. 2. Patient with PACG and others secondary glaucoma. 3. Patient underwent surgery on the inner eye 4. Patient who changed glaucoma treatment after ripasudil administration

Design outcomes

Primary

MeasureTime frame
measurement of IOPTimepoint: day 14, 1 month, 2months and 3 months

Secondary

MeasureTime frame
safety and tolerability of Ripasudil in comparison with TimololTimepoint: day 14, 1 month, 2 months and 3 months

Countries

India

Contacts

Public ContactDr Anitha S Maiya

JJMMC

dranithasmaiya@gmail.com9845467316

Outcome results

None listed

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