Effect of simple eye ointment on treatment of dry eye syndrome
Not Applicable
- Conditions
- dry eye syndrome.Lacrimal: cyst gland atrophy
- Registration Number
- IRCT2015090923952N1
- Lead Sponsor
- Vice Chancellery of Research of Semnan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients with DES clinical signs and symptoms which are confirmed by TBUT test; Patients must be between 20 and 60 years old; Patients must be diagnosed with DES for first time; Patients with idiopathic DES, not secondary types; Patients' workplace must be indoor; Patients must not take any ophthalmic drugs so far; Disease progression must be staged as mild or moderate; No history of undergoing refractive errors surgeries, utilizing contact eye lens and any drugs associated to DES; Informed consent for being involved in the study
Exclusion criteria: Refusal to keep participating in the study; Intolerance to treatment
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patients remission rate. Timepoint: before Intervention, 2 weeks after intervention and 4 weeks after intervention. Method of measurement: International Dry Eye Workshop(DEWS).
- Secondary Outcome Measures
Name Time Method Side effects of simple eye ointment. Timepoint: 1 month after intervention. Method of measurement: Standard questionnaire.