Effect of the Addition of Netarsudil 0.02% vs. Brimonidine 0.1% in Normal Tension Glaucoma Patients Currently on Latanoprost 0.005%

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

A randomized, multicenter, investigator-masked prospective study of NTG patients currently on latanoprost 0.005% monotherapy, to study the effect of IOP change with the introduction of netarsudil 0.02% vs brimonidine 0.1%. Subjects will be assessed at a screening visit, and 1 follow-up visit. Clinical evaluations will include visual acuity and IOP .

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Patients 18 years and older

• Diagnosed with normal tension glaucoma based on the following:

‣ IOP ≤ 21mmHg

⁃ Optic nerve rim thinning and/or retinal nerve fiber layer (RNFL) loss consistent with glaucoma

⁃ Normal visual field OR visual field loss consistent with optic nerve or RNFL defects within the last year

⁃ Open angles assessed by gonioscopy

• Have been on latanoprost monotherapy for at least 6 weeks

Locations
United States
Texas
Westlake Eye Specialists - Austin Office
RECRUITING
Austin
Westlake Eye Specialists - Killeen Office
RECRUITING
Killeen
Westlake Eye Specialists - Kyle Office
RECRUITING
Kyle
Westlake Eye Specialists - New Braunfels Office
RECRUITING
New Braunfels
Contact Information
Primary
Zarmeena Vendal, MD
zvendal@westlakeeyes.com
512-472-4011
Time Frame
Start Date: 2024-06-13
Estimated Completion Date: 2025-12-30
Participants
Target number of participants: 100
Treatments
Experimental: Netarsudil
netarsudil 0.02%
Active_comparator: Brimonidine
brimonidine 0.1%
Related Therapeutic Areas
Sponsors
Leads: Westlake Eye Specialists
Collaborators: Sengi

This content was sourced from clinicaltrials.gov