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Clinical Trial of Therapeutic Effect of Valproic Acid in Retinitis Pigmentosa

Clinical Trial of Therapeutic Effect of Valproic Acid in Retinitis Pigmentosa - VARP study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1091220053
Enrollment
30
Registered
2010-11-22
Start date
2010-12-24
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Retinitis Pigmentosa

Interventions

Intervention type:DRUG Name of intervention:Sodium valproate Dose form / Japanese Medical Device Nomenclature:TABLET Route of administration / Site of application:ORAL Dose per administration:200 0 mg

Sponsors

Yasuhiko Hirami
Lead Sponsor
Masayo Takahashi, Yasuo Kurimoto
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with Retinitis Pigmentosa with decreased visual acuity less than 0.7 and 0.1 or better in decimal visual acuity, and visual field less than 10 degrees by I-4 in Goldmann kinetic perimetry

Exclusion criteria

Exclusion criteria: 1) Patients with retinal degeneration secondary to ocular infection or inflammation 2) Patients with ocular disease other than Retinitis Pigmentosa 3) Patients with pregnancy or breast-feeding 4) Patients with abnormality in liver function or urea cycle 5) Patients with any drug allergy 6) Patients with bipolar disorder and suicide attempt 7) Patients using following drugs; carbapenem antibiotic, barbiturate, phenytoin, carbamazepine, ethosuximide, amitoripuchin, norutoripuchin, kuropazamu, lamotrigine, salicylic acid, benzodiazepines, warfarin, erythromycin, cimetidine, clonazepam 8) any other case that research physicians decided to be inappropriate for the study

Design outcomes

Primary

MeasureTime frame
Change in best corrected visual acuity

Countries

Japan

Contacts

Public ContactYasuhiko Hirami

Institute for Biomedical Research and Innovation Hospital

hirami@fbri.org+81-78-304-5200

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026