Trial · NCT07909720
The EYERISING Study
NCT07909720, Not applicable, Not yet recruiting, University of Wisconsin, Madison
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The EYERISING Study. Trials, record NCT07909720. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07909720
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The EYERISING Study
- NCT number
- NCT07909720
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 333 participants, estimated
- Lead sponsor
- University of Wisconsin, Madison
- Conditions
- Myopia, Astigmatism, Anisometropia
- Interventions
- Repeated Low-Level Red Light (RLRL) therapy, Placebo Device
- First posted
- 2026-11-02
- Last updated
- 2026-11-05
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in cycloplegic spherical equivalent refraction (SER) | Baseline, 4 months, 8 months, 12 months | SER will be measured using an autorefractometer after eye drops are given to temporarily relax the eye's focusing muscles. SER, measured in diopters (D), represents the amount of nearsightedness and will be used to measure the change in myopia from baseline. |
| Primary | Change in axial length (AL) | Baseline, 4 months, 8 months, 12 months | AL will be measured using the IOLMaster and reported in millimeters (mm). Change in AL from baseline will be used to assess ocular growth/myopia progression. |
| Secondary | Change in rate of SER increase | Baseline, 4 months, 8 months, 12 months | |
| Secondary | Change in rate of AL increase | Baseline, 4 months, 8 months, 12 months | |
| Secondary | Best corrected visual acuity (BCVA) | Baseline, 4 months, 8 months, 12 months | |
| Secondary | Change in National Eye Institute Visual Functioning Questionnaire (NEI VFQ-25) composite score | Baseline, 4 months, 8 months, 12 months | The NEI VFQ-25 is a 25-item questionnaire assessing vision-related functioning and quality of life. The composite score ranges from 0 to 100, with higher scores indicating better visual functioning and vision-related quality of life. |
| Secondary | Change in anterior chamber depth (ACD) | Baseline, 4 months, 8 months, 12 months | |
| Secondary | Change in corneal curvature (CC) | Baseline, 4 months, 8 months, 12 months | |
| Secondary | Change in choroidal thickness (CT) | Baseline, 4 months, 8 months, 12 months | |
| Secondary | Change in White-to-White (WTW) | Baseline, 4 months, 8 months, 12 months |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
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/NCT07909720
GET https://conductscience.org/api/trials/v1/NCT07909720/registered