Condition: Pigmentary Dispersion Syndrome · Pigmentary Dispersion Glaucoma · Sponsor: Mann Eye Institute
This study is a single-site, single-arm, prospective, observational study of IOP reduction after DSLT. Subjects will be assessed up to 12 months post-operatively. Clinical evaluations will include IOP and number of glaucoma medications.
This description comes directly from the study's public registry record.
Melissa Wright · 713-580-2500 · Melissa.Wright@manneye.com
Always discuss trial participation with your own doctor first.
| Mann Eye Institute | Houston, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07281391