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To study the role of oral valproic acid in patients with glaucoma

Effect of oral valproic acid in end stage glaucoma

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010510
Enrollment
60
Registered
2017-11-15
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: null- Glaucoma

Interventions

Intervention1: Valproic acid: Patients in intervention group will receive oral valproic acid 500mg OD for 3months (along with standard antiglaucoma medications, if needed) Control Intervention1: Cont

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. End stage glaucoma at least in one eye having a visual acuity of at least 6/36. (visual feild less than 10deg radius and mean deviation worse than 24dB) 2. IOP < 18 mm Hg on 2 consecutive visits (well controlled intraocular pressure)

Exclusion criteria

Exclusion criteria: 1. Patients with any other disease that might have contributed to visual field loss at the time of initial visual field test.(These diseases include other optic neuropathies, strokes, brain tumours, retinal vein or artery occlusion, macular disease including age-related macular degeneration, central retinal detachment and proliferative diabetic retinopathy.) 2. Patients already on oral valproic Acid for any other systemic illness. 3. Patients allergic to valproic acid, peanut oil. 4. Patients with deranged liver function test, hepatitis, alcoholic liver diseases. 5. Female patients in childbearing age , who did not undergo family planning.

Design outcomes

Primary

MeasureTime frame
Visual Acuity, Visual Field, Multifocal Electroretinigram.Timepoint: baseline, 3 months, 12 months.

Secondary

MeasureTime frame
Macular thicknessTimepoint: baseline,3 Months.

Countries

India

Contacts

Public ContactDr Karthikeyan Mahalingam

AIIMS

gupta_v20032000@yahoo.com01126593003

Outcome results

None listed

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