About this trial
The primary objective of this study is to determine if the addition of Rocklatan post-Hydrus will provide additional intraocular pressure lowering.
Eligibility criteria
Qualifiers
Age 40 years and older
Subjects who have mild to moderate Open Angle Glaucoma (OAG)
Subjects who have undergone uncomplicated cataract surgery and Hydrus microstent implantation > 3 months prior to screening and within the last 2 years
Post-Hydrus subjects on 0-2 ocular hypotensive medication classes who can safely washout (if on ocular hypotensive medications)
Disqualifiers
History of intraocular surgery except for uneventful refractive surgery or uncomplicated cataract surgery and hydrus microstent implantation
Prior Selective Laser Trabeculoplasty (SLT) within 18 months of surgery
Secondary glaucoma excluding pseudoexfoliation and pigmentary dispersion syndrome
Severe Open Angle Glaucoma
Trial design
Treatments tested in this trial
- Rocklatan (netarsudil 0.02% and latanoprost 0.005%)
- Systane