Status:
COMPLETED
Study of Tisporin Eye Drops Group and Restasis Eye Drops Group After Treatment, Each Treatment Group Comparisons for Evaluation of Efficacy and Safety in Moderate to Severe Dry Eye Disease
Lead Sponsor:
Hanlim Pharm. Co., Ltd.
Conditions:
Dry Eye Syndromes
Eligibility:
All Genders
21+ years
Phase:
PHASE3
Brief Summary
The purpose of this clinical Study is Tisporin Eye Drops 0.05%(Cyclosporine ophthalmic solution) group and Restasis Eye Drops 0.05%(Cyclosporine ophthalmic suspension) group 12 weeks after treatment, ...
Eligibility Criteria
Inclusion
- \[Patients with moderate-to-severe ocular dry eye\]
- The One eye of corneal fluorescein staining score of 2 or higher (Oxford grading)
- Non-anesthetic Schirmer test value ≤ 10mm/5min patients at least one eye score (Non-anesthetic Schirmer test value = 0/5min, nasal stimulation in the same eye, Schirmer test value ≥ 3mm/5min)
- Tear break-up time is 10 seconds or less
- Screening both eyes, the corrected visual acuity is 0.2 or more
- Despite conventional treatment, the symptoms of dry eye signs (Artificial tear eye drops, sympathetic nervous system stimulant agent, parasympathetic nerve stimulant, etc.)
Exclusion
- Screening visits in the previous 3 months (12 weeks) who participated in the clinical trials of cyclosporine eye drops, or if you used a cyclosporin ophthalmic solutions.
- The patients with systemic or ocular disorders affected the test results (ocular surgery, trauma, or disease)
- Abnormal eyelid function : Disoders of the eyelids or eyelashes
- Ocular allergies or currently under the treatment of allergic diseases of the eye (topical ocular mast cell stabilizer, antihistamine use, etc.)
- Cicatricial keratoconjunctivitis caused by herpetic keratopathy, conjunctival scarring (alkali damage, Steven-Johnson syndrome, cicatricial pemphigoid), pterygium, pinguecula, lack of congenital lacrimal, neurogenic keratitis, keratoconus, corneal transplantation
- current or recent patients used dry eye syndrome medications (topical or systemic) that may affect the status
- The use in clinical trials of drug hypersensitivity reactions in patients
Key Trial Info
Start Date :
December 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2014
Estimated Enrollment :
86 Patients enrolled
Trial Details
Trial ID
NCT02229955
Start Date
December 1 2013
End Date
July 1 2014
Last Update
September 3 2014
Active Locations (1)
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1
The catholic university of Korea seoul st. Mary's hospital
Seoul, Seocho-Ku, South Korea, 137-701