Rocklatan Adds Pressure Reduction After MIGS (Minimally Invasive Glaucoma Surgery)

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age40+
SponsorCenter for Sight Las Vegas

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

Treatment groups

68 Participants
are divided into 2 treatment groups

Sponsors and collaborators