Long-term Topical Cyclosporine for Atopic Keratoconjunctivitis
Primary Purpose
Atopic Keratoconjunctivitis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cyclosporin 0.05% ophthalmic
Sponsored by
About this trial
This is an interventional treatment trial for Atopic Keratoconjunctivitis focused on measuring Atopic, Keratoconjunctivitis, Restasis, Cyclosporine
Eligibility Criteria
Inclusion Criteria:
- Patient has known diagnosis of atopic keratoconjunctivitis
- Patient has been on cyclosporine 0.05% eye drops for control of atopic keratoconjunctivitis
- Patient has been followed up for at least for 1 year
- Patient is able to give informed consent
- Patient is able to tolerate a full ophthalmic exam
Exclusion Criteria:
- Patient has any other diagnosis (i.c. vernal keratoconjunctivitis, giant papillary conjunctivitis) that may alter the clinical appearance or behavior of their ocular surface)
Sites / Locations
- Johns Hopkins Hospital - Wilmer Eye Institute
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Cyclosporine 0.05% ophthalmic
Arm Description
cyclosporine 0.05% ophthalmic eye drops will be used starting with 1 drop in both eyes 6 times daily for first month, followed by 1 drop in both eyes 4 times daily for the following month, then will be adjusted by clinician as needed for appropriate disease control
Outcomes
Primary Outcome Measures
Ocular Symptoms and Signs Total Composite Score
Symptoms (itching, tearing, discomfort, discharge, photophobia) and signs (Bulbar conjunctival hyperemia, upper tarsal conjunctival papillae, punctate keratitis, corneal neovascularization, cicatrizing conjunctivitis, and blepharitis) evaluated on a 4 point scale of 0-3, with a minimum symptom score of 0- maximum 15, and sign score minimum 0- maximum 18. These scores are combined to yeild a total composite score of signs and symptoms of minimum 0-maximum 33. The highest score would indicate the most severe case of Atopic Keratoconjunctivitis (AKC). The composite score is reported.
Secondary Outcome Measures
Corticosteroid Usage
Number of flare-ups requiring topical steroid-use across all participants over the entire 12 month follow-up period
Full Information
NCT ID
NCT00987467
First Posted
September 30, 2009
Last Updated
March 6, 2018
Sponsor
Johns Hopkins University
1. Study Identification
Unique Protocol Identification Number
NCT00987467
Brief Title
Long-term Topical Cyclosporine for Atopic Keratoconjunctivitis
Official Title
Long-term Results of Topical Cyclosporine 0.05% in the Treatment of Atopic Keratoconjunctivitis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
September 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Atopic keratoconjunctivitis (AKC) is a rare type of ocular allergy that is often associated with eczema. Over time, the complications from this disease process lead to loss of vision due to continual scarring of the corneal surface. The pathophysiology of AKC has not been fully elucidated, and the triggers are still unknown.
Corticosteroids are very effective in controlling the acute symptoms of AKC. However, two thirds of patients managed with a combination of oral antihistamine, topical mast cell stabilizer, and intermittent topical steroid regimen eventually developed significant keratopathy and vision loss. Additionally, there are many side effects of corticosteroids, including local immunosuppression, cataract formation, and increased risk of glaucoma.
Cyclosporin A is an immunomodulator that specifically inhibits T lymphocytes by blocking the expression of the interleukin-2 receptor. It also blocks the release of inflammatory mediators from mast cells and eosinophils. Cyclosporin has no known side effects except for burning upon instillation, and safe to use over long-term . The investigators have demonstrated that a 0.05% ophthalmic emulsion of cyclosporine has been shown to be effective at improving the ocular signs and symptoms of AKC over short-term. However, the long-term efficacy of cyclosporine A in slowing the natural history of AKC and possible steroid sparing effects have not been assessed. The investigators hypothesize that cyclosporine A can be used as a mainstay treatment of AKC to control signs and symptoms over a long period of time and also prevent the progression of this disease.
Detailed Description
Atopic keratoconjunctivitis (AKC) is a rare type of ocular allergy that is often associated with eczema. Over time, the complications from this disease process lead to loss of vision due to continual scarring of the corneal surface. The pathophysiology of AKC has not been fully elucidated, and the triggers are still unknown.
Corticosteroids are very effective in controlling the acute symptoms of AKC. However, two thirds of patients managed with a combination of oral antihistamine, topical mast cell stabilizer, and intermittent topical steroid regimen eventually developed significant keratopathy and vision loss. Additionally, there are many side effects of corticosteroids, including local immunosuppression, cataract formation, and increased risk of glaucoma.
Cyclosporin A is an immunomodulator that specifically inhibits T lymphocytes by blocking the expression of the interleukin-2 receptor. It also blocks the release of inflammatory mediators from mast cells and eosinophils. Cyclosporin has no known side effects except for burning upon instillation, and safe to use over long-term . The investigators have demonstrated that a 0.05% ophthalmic emulsion of cyclosporine has been shown to be effective at improving the ocular signs and symptoms of AKC over short-term. However, the long-term efficacy of cyclosporine A in slowing the natural history of AKC and possible steroid sparing effects have not been assessed. The investigators hypothesize that cyclosporine A can be used as a mainstay treatment of AKC to control signs and symptoms over a long period of time and also prevent the progression of this disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Keratoconjunctivitis
Keywords
Atopic, Keratoconjunctivitis, Restasis, Cyclosporine
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cyclosporine 0.05% ophthalmic
Arm Type
Experimental
Arm Description
cyclosporine 0.05% ophthalmic eye drops will be used starting with 1 drop in both eyes 6 times daily for first month, followed by 1 drop in both eyes 4 times daily for the following month, then will be adjusted by clinician as needed for appropriate disease control
Intervention Type
Drug
Intervention Name(s)
Cyclosporin 0.05% ophthalmic
Other Intervention Name(s)
Restasis
Intervention Description
Cyclosporine 0.05% ophthalmic solution, 1 drop 6 times in both eyes daily for first month, then 1 drop 4 times in both eyes daily for next month, then dosage was adjusted based on clinical disease by investigator.
Primary Outcome Measure Information:
Title
Ocular Symptoms and Signs Total Composite Score
Description
Symptoms (itching, tearing, discomfort, discharge, photophobia) and signs (Bulbar conjunctival hyperemia, upper tarsal conjunctival papillae, punctate keratitis, corneal neovascularization, cicatrizing conjunctivitis, and blepharitis) evaluated on a 4 point scale of 0-3, with a minimum symptom score of 0- maximum 15, and sign score minimum 0- maximum 18. These scores are combined to yeild a total composite score of signs and symptoms of minimum 0-maximum 33. The highest score would indicate the most severe case of Atopic Keratoconjunctivitis (AKC). The composite score is reported.
Time Frame
Baseline and 8 weeks
Secondary Outcome Measure Information:
Title
Corticosteroid Usage
Description
Number of flare-ups requiring topical steroid-use across all participants over the entire 12 month follow-up period
Time Frame
Entire follow-up period (Approximately 12 months)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient has known diagnosis of atopic keratoconjunctivitis
Patient has been on cyclosporine 0.05% eye drops for control of atopic keratoconjunctivitis
Patient has been followed up for at least for 1 year
Patient is able to give informed consent
Patient is able to tolerate a full ophthalmic exam
Exclusion Criteria:
Patient has any other diagnosis (i.c. vernal keratoconjunctivitis, giant papillary conjunctivitis) that may alter the clinical appearance or behavior of their ocular surface)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Esen K Akpek, MD
Organizational Affiliation
Johns Hopkins Hospital - Wilmer Eye Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Hospital - Wilmer Eye Institute
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
15019322
Citation
Akpek EK, Dart JK, Watson S, Christen W, Dursun D, Yoo S, O'Brien TP, Schein OD, Gottsch JD. A randomized trial of topical cyclosporin 0.05% in topical steroid-resistant atopic keratoconjunctivitis. Ophthalmology. 2004 Mar;111(3):476-82. doi: 10.1016/j.ophtha.2003.05.035.
Results Reference
background
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Long-term Topical Cyclosporine for Atopic Keratoconjunctivitis
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