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Trial · NCT01190306

Safety Study of the VEGA UV-A System to Treat Keratoconus

NCT01190306, Phase 3, Terminated, Topcon Medical Systems, Inc.; results first posted 2013-03-04

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Safety Study of the VEGA UV-A System to Treat Keratoconus. Trials, record NCT01190306. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01190306

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Safety Study of the VEGA UV-A System to Treat Keratoconus
NCT number
NCT01190306
Status
Terminated
Phases
Phase 3
Enrollment
127 participants, actual
Lead sponsor
Topcon Medical Systems, Inc.
Conditions
Keratoconus
Interventions
The VEGA UV-A Illumination System, Riboflavin
First posted
2010-08-27
Last updated
2022-07-12
Results first posted
2013-03-04

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Corneal Curvature.6 Months

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Corneal Curvature.6 Months
The CXL-001 study was completed but data analysis was not done. Prior to data analysis, the sponsor, Topcon, decided to terminate the study for administrative reasons only, and not as a result of any safety issues or concerns relating to the study.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCXL Treatment61
Overall StudySTARTEDSham Control66
Overall StudyCOMPLETEDCXL Treatment61
Overall StudyCOMPLETEDSham Control66
Overall StudyNOT COMPLETEDCXL Treatment0
Overall StudyNOT COMPLETEDSham Control0

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCXL Treatment
Total, all-cause mortalitySham Control
Total, other adverse eventsCXL Treatment061
Total, other adverse eventsSham Control066
Total, serious adverse eventsCXL Treatment061
Total, serious adverse eventsSham Control066

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
CXL Treatment vs Sham Control: serious adverse events

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT01190306

GET https://conductscience.org/api/trials/v1/NCT01190306/registered