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Role of topical brinzolamide in infantile nystagmus syndrome

Not Applicable
Completed
Conditions
Health Condition 1: null- Patients of infantile nystagmus syndrome will be included.
Registration Number
CTRI/2018/05/014335
Lead Sponsor
Pharmacology department RPC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
29
Inclusion Criteria

1.Informed consent from self or guardian(in case of minor)

2.Subjects will have INS diagnosed by clinical evaluation and eye movement recordings

3.will be >=10 years of age

4.will able to make the required study visits.

Exclusion Criteria

1.Current or within the last 12 months use of medications for nystagmus, history of any ocular surgery.

2.Any systemic diseases requiring medication known to affect the ocular motor system

3.Behavioural or neurological disorders which would interfere with the study

4.Pregnancy,nursing or planning of a pregnancy and

5.Known allergy to brinzolamide

6.Participation in any study involving an investigational new drug within the past year

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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