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A study to compare the clinical efficacy and quality of life in patients after treatment with cyclosporine eye drops versus chloroquine eye drops in dry eye disease.

A comparative study of the clinical efficacy and quality of life in patients after treatment with topical cyclosporine versus topical chloroquine in moderate to severe dry eye disease. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072597
Enrollment
100
Registered
2024-08-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H188- Other specified disorders of cornea

Interventions

Intervention1: Chloroquine 0.03% eye drops: Topical eye drops two times a day for one month. Control Intervention1: Cyclosporine 0.05% eye drops: Topical eye drops two times a day for one month. Contr

Sponsors

Dr Ekroop Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with symptoms of moderate to severe dry eye. Patients with findings of dry eye on slit lamp examination.

Exclusion criteria

Exclusion criteria: Patients with history of ocular surgery or ocular trauma in last 2 months. Patients with history of contact lens use in last 2 months. Patients with active ocular disease other than dry eye like uveitis, keratitis, conjunctivitis etc. Patients allergic to fluorescein stain. Patients with history of allergy to either of the test drugs. Patients unable to undergo Schirmer’s test or slit lamp examination and hence TBUT. Patients unable to understand regional language or English and hence understand OSDI questionnaire. Pregnant females.

Design outcomes

Primary

MeasureTime frame
Assessment and comparison of clinical efficacy of topical chloroquine 0.03% versus topical cyclosporine 0.05% in patients with moderate to severe dry eye disease by means of testing for Schirmer test, Tear film breakup time and OSDI score.Timepoint: 1 month

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDR EKROOP KAUR

Guru Gobind Singh Medical College and Hospital, Faridkot 151203, Punjab, India

neha.knew@gmail.com7009909238

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026