Clinical Trials Directory

Trials / Unknown

UnknownNCT00739154

Protective Effect of Phenytoin on Glaucoma

Clinical Cohort Study of Association Between Steady State Phenytoin Treatment and Better Clinical Parameters of Glaucoma

Status
Unknown
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Rabin Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

since glaucoma is considered an optic neuropathy, new treatments for glaucoma are being continuously investigated, including neuroprotection. Previous studies implied that phenytoin, a potent anti-convulsive drug, has a neuroprotective role, and Na+ channels blockage was suggested as a possible mechanism. This study predicts that glaucoma patients taking Phenytoin will have a less advanced glaucoma as compared to patients not taking the drug. Glaucoma severity will be determined by visual acuity, visual fields, optic disc cupping and nerve fiber layer thickness

Detailed description

The study will examine adult patients who suffer from glaucoma and epileptic disorders on the same time. the study group will include glaucoma patients, being treated with oral Phenytoin for their epileptic disorder. The study group will be compared to 2 control groups: * Glaucoma patients with epileptic disorder,receiving different medication than Phenytoin * Glaucoma patients with no epileptic disorder. 4 parameters will be evaluated for all groups: 1. Best corrected visual acuity 2. Optic disc cupping 3. visual fields and general perimetric indices 4. peripapillary retinal nerve fiber layer. Every participant in the study,after giving his informed consent, will be evaluated by a senior ophthalmologist in a single office appointment. The appointment will include a visual acuity, complete ophthalmic examination,Humphrey perimetric visual field testing and peripapillary RNFL thickness measurement by OCT. no drug or other treatment will be given to the participants after data collection, average +/-Standard deviation for the 4 parameters will be compared between the 3 groups. Student T-test and one- way ANOVA will be used for statistical analysis.

Conditions

Timeline

Start date
2008-11-01
Primary completion
2010-11-01
Completion
2010-12-01
First posted
2008-08-21
Last updated
2008-08-21

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00739154. Inclusion in this directory is not an endorsement.