Overview
Vigamox Treatment for Ocular Graft-Versus-Host Disease
Status:
Recruiting
Recruiting
Trial end date:
2022-07-31
2022-07-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
In this study the investigators seek to prospectively measure the response of ocular graft-versus-host disease (GVHD) patients to treatment with topical Vigamox. The investigators will accomplish this by enrolling patients with bilateral ocular GVHD and treating one eye with topical Vigamox and the other eye with a placebo eye drop. By assessing the response to treatment with Vigamox, the investigators hope to identify a role for topical antibiotic treatment in ocular GVHD.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Washington University School of MedicineTreatments:
MoxifloxacinNorgestimate, ethinyl estradiol drug combination
Criteria
Inclusion Criteria:-Participants will be adults with a history of allogeneic hematopoietic stem cell
transplantation, signs of either acute or chronic GVHD per the hematologist, signs and
symptoms consistent with ocular GVHD + within 4 months of developing symptoms of ocular
GVHD
Exclusion Criteria:
- Treated with antibiotic eye drops in the month prior to enrollment
- History of fluoroquinolone allergy
- Asymmetric ocular disease
- Pregnant
- Nursing