Dry Eyes Clinical Trial
— Lotemax_BMTOfficial title:
Treatment of Ocular Graft-versus-Host Disease (GVHD) With Topical Loteprednol
Verified date | August 2015 |
Source | University of Michigan |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The purpose of this research is to:
1. 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.
2. 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.
3. 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.
Status | Completed |
Enrollment | 75 |
Est. completion date | February 2015 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Scheduled for allogenic bone marrow transplant Exclusion Criteria: Allergic reaction to loteprednol or cyclosporine, previous allogenic transplant |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Michigan | Bausch & Lomb Incorporated |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | 1 year | No |
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