Overview

Effect of Levodopa-Carbidopa on Visual Function in Patients With Recent-Onset Nonarteritic Anterior Ischemic Optic Neuropathy

Status:
Completed
Trial end date:
2003-04-01
Target enrollment:
0
Participant gender:
All
Summary
Purpose: There are some controversies about the effect of Levodopa-Carbidopa on treatment of non-arteritic anterior ischemic optic neuropathy (NAION). This study was performed to evaluate the effect of Levodopa-Carbidopa on visual acuity, color vision, and visual field in patients with recent onset NAION (less than 6 weeks duration). Patients and Methods: In this double-blind randomized clinical trial, 13 patients were treated with levodopa-carbidopa and 12 patients took placebo for 3 weeks. Visual acuity, color vision, and visual field were tested before and at 4th, 12th, 16th, and 24th weeks after enrollment, and evaluated.
Phase:
Phase 4
Details
Lead Sponsor:
Shahid Beheshti University of Medical Sciences
Treatments:
Carbidopa
Carbidopa, levodopa drug combination
Levodopa
Criteria
Inclusion Criteria:

- age greater than 50 years old

- first ophthalmic examination within 6 weeks after onset of disease

- presence of optic disc swelling followed by optic atrophy within 6 weeks

- altitudinal, central or generalized visual field defect

- normal ESR

Exclusion Criteria:

- confirmed giant cell arteritis

- history of any ocular surgeries

- optic neuropathy due to acute bleeding

- advanced diabetic retinopathy

- uncontrolled glaucoma

- any ocular disorders that cause visual acuity reduction rather than NAION