NCT07847073RecruitingPhase 4
Adaptive Optics OCT Evaluation of Rhopressa's Effects on the Retinal Ganglion Cells in Glaucoma Patients
Source: ClinicalTrials.gov · Last updated 28 Oct 2026
Brief summary (registry, in English)
The purpose of this study is to compare how two FDA-approved eye drops: netarsudil (Rhopressa) and timolol, protect nerve cells in the eye of adults with open-angle glaucoma. Both medications lower pressure inside the eye, but researchers want to learn if Rhopressa is more effective at slowing down or preventing the loss of retinal ganglion cells. These cells are essential for sight because they carry visual signals from the eye to the brain. Participants in this study will complete a total of 6 study visits over 12 months: * Participants will spend 6 months using Rhopressa eye drops and 6 months using Timolol eye drops. The order of the two eye drops will be chosen randomly. * At scheduled study visits, researchers will examine participants' eyes and measure eye pressure. * Researchers will take detailed pictures of the back of the eye using a specialized high-resolution camera called adaptive optics optical coherence tomography (AO-OCT). * Participants will also complete specialized visual field testing to measure eye function. Researchers will count and track individual nerve cells over time to determine if one medication offers better protection against cell loss than the other.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 13 (estimated)
- First submitted
- 22 Sept 2026
- Start date
- 1 Oct 2026
- Primary completion date
- 31 Jan 2028
- Lead sponsor
- Brett King
- Diseases
- Glaucoma
- NCT number
- NCT07847073
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 13
- From 1 Oct 2026 to the primary completion date, 31 Jan 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Any subject whom the investigator determines to be at unacceptable risk for the washout or believes is unlikely to complete the study
Other illness
- Subjects with retinal disease or optic neuropathies other than glaucoma that, in the opinion of the investigator, could confound the study assessments or outcome
Age
- Female subjects who are pregnant, breastfeeding, or of childbearing age who are not sterile or using an acceptable method of contraception during the study
Other
- Subjects with a known intolerance to netarsudil ophthalmic solution
- Subjects with a known intolerance to, or contraindication for, timolol maleate
Who the study is looking for
- All subjects will be 18 years of age or older
- Subjects must be diagnosed with open-angle glaucoma and have had an eye exam within the past year
- Subjects with glaucoma will have structural (optic nerve and retinal nerve fiber layer) and functional (visual field testing) defects consistent with the diagnosis of glaucoma
- Subjects will have a corrected acuity of 20/50 or better and be able to fixate
- Naïve to medication subjects or post washout IOP between 18 and 34 mmHg
- Spherical equivalent from +3 diopters to -6 diopters, with a cylinder of \<-3 diopters
- Subject is willing and able to comply with the protocol requirements and to remain in the study for its full duration, including all scheduled visits and follow-up assessments
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Indiana University School Of Optometry Coordinator of this site? Confirm its status | Bloomington | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.