Treatment of Ocular Graft-versus-Host Disease (GVHD) With Topical Loteprednol Etabonate 0.5% (Lotemax_BMT)
Primary Purpose
Dry Eyes
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Lotemax
Restasis
Sponsored by
About this trial
This is an interventional prevention trial for Dry Eyes focused on measuring Graft versus Host Disease (GVHD), dry eyes, Bone marrow transplant (BMT), Restasis, Lotemax
Eligibility Criteria
Inclusion Criteria:
Scheduled for allogenic bone marrow transplant
Exclusion Criteria:
Allergic reaction to loteprednol or cyclosporine, previous allogenic transplant
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Lotemax
Restasis
Arm Description
Loteprednol Etabonate 0.5%
Cyclosporine
Outcomes
Primary Outcome Measures
Progression of Dry Eye Severity
Dry eye is one of the major symptoms of ocular GVHD in bone-marrow transplant recipients, worsening of dry eye symptoms may be indicative of worsening ocular GVHD conditions.
Secondary Outcome Measures
Full Information
NCT ID
NCT01695668
First Posted
September 25, 2012
Last Updated
August 24, 2015
Sponsor
University of Michigan
Collaborators
Bausch & Lomb Incorporated
1. Study Identification
Unique Protocol Identification Number
NCT01695668
Brief Title
Treatment of Ocular Graft-versus-Host Disease (GVHD) With Topical Loteprednol Etabonate 0.5%
Acronym
Lotemax_BMT
Official Title
Treatment of Ocular Graft-versus-Host Disease (GVHD) With Topical Loteprednol
Study Type
Interventional
2. Study Status
Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
February 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
Bausch & Lomb Incorporated
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this research is to:
Evaluate the safety and efficacy of a steroid eye drop (Lotemax) in patients who have been diagnosed with graft-versus-host disease (GVHD), which is a complication that may occur after bone marrow transplant where the newly transplanted material attacks the patient's body and may cause eye dryness.
Assess the safety and efficacy of Lotemax in decreasing the eye's reaction to the process in GVHD before the patient undergoes bone marrow transplant.
Compare how well Lotemax works in decreasing the process in GVHD with an immunosuppressive eye drop (Restasis), which has been commonly used in the treatment of this condition.
Detailed Description
Allogeneic bone marrow or peripheral stem cell transplantation result in Graft-versus-Host disease. Ocular symptoms may be the first presentation of GVHD and may be seen in the absence of systemic manifestations. GVHD is categorized into acute and chronic forms as defined by 100 days after the transplant. Acute GVHD is characterized by dermatitis, hepatitis, and enteritis. Chronic GVHD involves the skin, mouth, liver, gastrointestinal tract, lungs, and eyes. Ocular GVHD is a common cause of dry eye symptoms in patients who have undergone bone marrow transplant (BMT), and can be defined as ocular surface disease in the context of GVHD. Dry eyes develop in 76% of acute GVHD patients and between 62.5% and 81.8% of chronic GVHD patients. Current treatment for ocular GVHD includes topical cyclosporine 0.05% (Restasis, Allergan). Topical loteprednol etabonate 0.5% (Lotemax, Bausch and Lomb) has been shown to be safe and efficacious in treatment of inflammatory ocular disorders, but has not been prospectively studied in ocular GVHD.
2. Hypothesis: We anticipate that topical loteprednol etabonate 0.5% will be safe and efficacious in treatment of ocular GVHD patients, and would add to the armamentarium of therapeutics for this disease. Further, by following the natural progression of the disease prior to a patient's Bone Marrow Transplant (BMT), we may elucidate a new standard of care for these patients - one that involves referral to an ophthalmologist before ocular GVHD symptoms arise.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eyes
Keywords
Graft versus Host Disease (GVHD), dry eyes, Bone marrow transplant (BMT), Restasis, Lotemax
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lotemax
Arm Type
Experimental
Arm Description
Loteprednol Etabonate 0.5%
Arm Title
Restasis
Arm Type
Active Comparator
Arm Description
Cyclosporine
Intervention Type
Drug
Intervention Name(s)
Lotemax
Other Intervention Name(s)
Loteprednol
Intervention Description
Ophthalmic corticosteroid. It decreases inflammation of the eye
Intervention Type
Drug
Intervention Name(s)
Restasis
Other Intervention Name(s)
cyclosporine
Intervention Description
Restasis is an immunosuppressive agent. Cyclosporine may reduce inflammation in the eye.
Primary Outcome Measure Information:
Title
Progression of Dry Eye Severity
Description
Dry eye is one of the major symptoms of ocular GVHD in bone-marrow transplant recipients, worsening of dry eye symptoms may be indicative of worsening ocular GVHD conditions.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Scheduled for allogenic bone marrow transplant
Exclusion Criteria:
Allergic reaction to loteprednol or cyclosporine, previous allogenic transplant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shahzad Mian, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Treatment of Ocular Graft-versus-Host Disease (GVHD) With Topical Loteprednol Etabonate 0.5%
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