Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease
Primary Purpose
Primary Sjogren Syndrome, Secondary Sjogren Syndrome, Aqueous Deficient Dry Eye Disease
Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Restasis
Refresh Endura
Sponsored by
About this trial
This is an interventional treatment trial for Primary Sjogren Syndrome focused on measuring Evaporative, Aqueous deficient, Dry eye disease
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed for mild to moderate Aqueous Deficient DED (ADDED), defined as Schirmer 1 < 10mm;
- Patients diagnosed for mild to moderate Evaporative DED (EDED), defined as normal Schirmer 1 and BUT < 5 seconds;
- Patients submitted to refractive surgery,
- Patients capable of understanding instructions, signing the term of consent and available to attend all exam visits.
Exclusion Criteria:
- patients with punctual occlusion,
- active ocular infection or inflammatory disease,
- history of herpetic keratitis,
- contact lens use during trial period,
- patients with glaucoma,
- any eyelid globe malposition abnormality.
Sites / Locations
- Departamento de Oftalmologia da Escola Paulista de Medicina - UNIFESP
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Refresh Endura
Restasis
Arm Description
Topical lubricant containing (glycerin; polysorbate 80; castor oil; carbomer, boric acid, sodium hydroxide, purified water), one drop 2 times a day, for 3 months.
Topical immunomodulatory lubricant (Ophthalmic emulsion containing cyclosporine 0.5 mg/mL, i.e., 0.05%), one drop 2 times a day, for 3 months
Outcomes
Primary Outcome Measures
Ocular surface inflammation
Secondary Outcome Measures
Full Information
NCT ID
NCT02004067
First Posted
December 3, 2013
Last Updated
September 20, 2020
Sponsor
Federal University of São Paulo
Collaborators
Allergan
1. Study Identification
Unique Protocol Identification Number
NCT02004067
Brief Title
Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease
Official Title
Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of São Paulo
Collaborators
Allergan
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In the present study the investigators aim to determine the efficacy of an immunomodulating topical medication, compared with a topical lubricant, on the treatment of dry eye disease (DED) due to primary or secondary Sjögren's syndrome (aqueous deficient DED) and evaporative DED.
Detailed Description
Dry eye disease (DED) is a multifactorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability with potential damage to the ocular surface. It is accompanied by increased osmolarity of the tear film and inflammation of the ocular surface. DED prevalence is estimated around 15 -35% of the population over 50 years old. There is a wide variety of topic medications for the treatment of DED, though few aim the re-establishment of tear osmolarity equilibrium and reduction of damages to the ocular surface. The treatment of DED can include a medical treatment, such as tear substitution, tear preservation, production stimulation, anti-inflammatory; it can also include surgical treatment, as tarsorrhaphy and salivary gland transplant. Considering tear substitutes and anti-inflammatory topical treatments, the purpose of our study is to determine efficacy of an immunomodulating topical medication containing 0.05% cyclosporine A (CsA), compared to a topical lubricant (vitamin A, Refresh Endura®), on the treatment of dry eye disease (DED) due to primary or secondary Sjögren's syndrome (aqueous deficient DED) and evaporative DED.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Sjogren Syndrome, Secondary Sjogren Syndrome, Aqueous Deficient Dry Eye Disease, Evaporative Dry Eye Disease
Keywords
Evaporative, Aqueous deficient, Dry eye disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Refresh Endura
Arm Type
Active Comparator
Arm Description
Topical lubricant containing (glycerin; polysorbate 80; castor oil; carbomer, boric acid, sodium hydroxide, purified water), one drop 2 times a day, for 3 months.
Arm Title
Restasis
Arm Type
Experimental
Arm Description
Topical immunomodulatory lubricant (Ophthalmic emulsion containing cyclosporine 0.5 mg/mL, i.e., 0.05%), one drop 2 times a day, for 3 months
Intervention Type
Drug
Intervention Name(s)
Restasis
Other Intervention Name(s)
Cyclosporine 0.05%
Intervention Description
Restasis is an ophthalmic emulsion containing cyclosporine 0.5 mg/mL, produced by Allergan Inc.
Intervention Type
Drug
Intervention Name(s)
Refresh Endura
Other Intervention Name(s)
Castor oil
Intervention Description
Refresh Endura is a topical lubricant produced by Allergan, Inc.
Primary Outcome Measure Information:
Title
Ocular surface inflammation
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed for mild to moderate Aqueous Deficient DED (ADDED), defined as Schirmer 1 < 10mm;
Patients diagnosed for mild to moderate Evaporative DED (EDED), defined as normal Schirmer 1 and BUT < 5 seconds;
Patients submitted to refractive surgery,
Patients capable of understanding instructions, signing the term of consent and available to attend all exam visits.
Exclusion Criteria:
patients with punctual occlusion,
active ocular infection or inflammatory disease,
history of herpetic keratitis,
contact lens use during trial period,
patients with glaucoma,
any eyelid globe malposition abnormality.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rossen M Hazarbassanov, PhD
Organizational Affiliation
Federal University of São Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departamento de Oftalmologia da Escola Paulista de Medicina - UNIFESP
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
04023 062
Country
Brazil
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Disease
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