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Impact of tacrolimus 0.03% eye drop on dry eye symptoms

Comparing the effect of tacrolimus 0.03% drop and artificial tear drop on the amount of tear production in patients with dry eye after cataract surgery with phacoemulsification method.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016102430485N1
Enrollment
60
Registered
2017-03-27
Start date
2016-10-29
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

dry eye syndrome. Other disorders of lacrimal gland

Interventions

Intervention 1: Intervention group: The first patient with a unique code (1) would be given package A (include tacrolimus 0.03% drop). Patients would instil tacrolimus 0.03% drop every 12 hours a day
Treatment - Drugs
Intervention group: The first patient with a unique code (1) would be given package A (include tacrolimus 0.03% drop). Patients would instil tacrolimus 0.03% drop every 12 hours a day for one month. P
Control group: The second patient with a unique code (2) would be given package B (include artificial tear drop). Patients would instil a drop of artificial tear drop, with trademark of Artelac, in ey

Sponsors

Vice Chancellor for research of Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients aged above 50 years old with cataract planned for phacoemulsification. Exclusion criteria: history of an ocular trauma or any chemical or thermal burn; allergy to any of the study medications; history of any condition that may cause dry eye; systemic connective tissue disease; corneal contact lens wear; any active ocular disease; uncontrolled systemic disease; a history of ocular allergic disease; prior refractive surgery or any ocular surgery; history of any medication which may induce dry eye; any history of inflammatory or infectious ocular disease; diagnosis of dry eye syndrome by Schirmer 1 test <10 mm or tear film break up time <10 seconds.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Eye problems in doing daily jobs. Timepoint: Before intervention and one month after treatment. Method of measurement: Ocular Surface Disease Index questionnaire.;Tear break up time. Timepoint: Before intervention and one month after treatment. Method of measurement: In seconds, With timer and Slit Lamp.;Tear production. Timepoint: Before intervention and one month after treatment. Method of measurement: Schirmer 1 test in millimeters.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArmin Hemati

Yazd University of Medical Sciences

armin7hemati@gmail.com+98 35 3822 4002

Outcome results

None listed

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