Trial · NCT07048886
Rocklatan Adds Pressure Reduction After MIGS (Minimally Invasive Glaucoma Surgery)
NCT07048886, Phase 4, Not yet recruiting, Center for Sight Las Vegas
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Rocklatan Adds Pressure Reduction After MIGS (Minimally Invasive Glaucoma Surgery). Trials, record NCT07048886. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07048886
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Rocklatan Adds Pressure Reduction After MIGS (Minimally Invasive Glaucoma Surgery)
- NCT number
- NCT07048886
- Status
- Not yet recruiting
- Phases
- Phase 4
- Enrollment
- 68 participants, estimated
- Lead sponsor
- Center for Sight Las Vegas
- Conditions
- Primary Open Angle Glaucoma
- Interventions
- Rocklatan (netarsudil 0.02% and latanoprost 0.005%), Systane
- First posted
- 2025-07-03
- Last updated
- 2025-07-03
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean diurnal intraocular pressure change from baseline | After 28 days up to 35 days post initiation of Rocklatan vs placebo comparator | After Hydrus prior to study initiation drop |
| Secondary | Diurnal Intraocular pressure change from baseline and difference between intraocular pressure at each time point | After Hydrus prior to study drop and after 28 days up to 35 days post initiation of study drop for all time points 8am, 10am, 4pm (± 1 hour) between groups | Goldmann Applanation Tonometry |
| Other | Change in corneal hysteresis from baseline | Change from baseline after 28 days up to 35 days post initiation of study drop | Ocular Response Analyzer |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07048886
GET https://conductscience.org/api/trials/v1/NCT07048886/registered