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Effect of two different doses of Tacrolimus eye ointment in Chronic allergic Conjunctivitis

Phase 3
Conditions
Health Condition 1: H104- Chronic conjunctivitis
Registration Number
CTRI/2023/09/057951
Lead Sponsor
KAHER JGMM Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Age >14yrs

2.Active bilateral severe VKC responding poorly despite >1 month of treatment with topical anti allergic agents and corticosteroids.

Exclusion Criteria

1.Patients with adnexal abnormalities, glaucoma, contact lens wearer, corneal pathology will be excluded from the study.

2.Patients who have received immunosuppressive therapy

3.Patients with known hypersensitivity to Tacrolimus eye ointment

4.Pregnant and lactating women will be excluded from the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in mean scores of ocular symptoms and signs at 2nd week, 4th week, 6th week and 8th week from baseline. <br/ ><br>Timepoint: <br/ ><br>All the parameters will be evaluated at baseline visit, day 14, day 30 & day 45.
Secondary Outcome Measures
NameTimeMethod
Secondary outcome measures: <br/ ><br>1.Subjective scoring of symptoms at baseline, 2nd week, 4th week, 6th week & 8th week. <br/ ><br>2.Any adverse effects from the treatment reported. <br/ ><br>Timepoint: All the parameters will be evaluated at baseline visit, day 14, day 30 & day 45.
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