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

Part of paid clinical trials in Las Vegas, Nevada.

Sponsor
Center for Sight Las Vegas
Study ID
NCT07048886
Phase
PHASE4
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Primary Open Angle Glaucoma

Eligibility Criteria

Sex
ALL
Age
40 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Rocklatan (netarsudil 0.02% and latanoprost 0.005%) — DRUG
    Additional intraocular eye pressure lowering post-Hydrus
  • Systane — DRUG
    Placebo Comparator (artificial tears)

Study Details

The primary objective of this study is to determine if the addition of Rocklatan post-Hydrus will provide additional intraocular pressure lowering.

Key Dates

Start date
Jul 15, 2025
Status verified
Jun 2025
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
68 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Placebo Comparator: Placebo Comparator Systane Artificial Tears
    Comparator arm is Systane artificial tears
  • Active Comparator: FDA Approved Rocklatan (netarsudil 0.02% and latanoprost 0.005%)
    FDA approved Rocklatan (netarsudil 0.02% and latanoprost 0.005%) is a fixed dose combination of a Rho kinase inhibitor and a prostaglandin analogue indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

Primary Outcome Measure

Mean diurnal intraocular pressure change from baseline [ Time Frame: After 28 days up to 35 days post initiation of Rocklatan vs placebo comparator ]

Central Contacts

  • Clinical Research Manager
    702-724-2005
  • Clinical Research Coordinator
    702-724-2067

Locations (1)

FacilityCityStateZIPSite coordinators
Center for SightLas VegasNevada89145
Clinical Research Manager
702-724-2005
Clinical Research Coordinator

Find similar trials in Las Vegas, NV

Related Studies