None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All young adult patients [18 years to 30 years], presented with dry eye disease and also having concurrent Acne vulgaris and providing written consent for voluntary participation would be recruited for this study.
Exclusion criteria
Exclusion criteria: subjects with any known systemic illnesses like diabetes mellitus, thyroid disorders and auto-immune disorders. Subjects with history of smoking, alcohol consumption, or any other drugs like isotretonion, anti-histaminic, anti-cancer and beta-blockers would be excluded. Subjects with Computer work or mobile use of more than four hours in a day would also be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the clinical efficacy of oral Zinc supplement with the conventional treatment in young adult patients of dry eye disease associated with acne vulgaris.Timepoint: Two years | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Objectives To compare the treatment response in terms of duration of treatment To compare the treatment response in terms of fastest clinical response.Timepoint: two years | — |
Countries
India
Contacts
AIIMS Deoghar