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Comparison · NCT03292809-sae

CyclASol Ophthalmic Solution vs Vehicle Ophthalmic Solution: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. CyclASol Ophthalmic Solution vs Vehicle Ophthalmic Solution: serious adverse events. Trial comparisons, record NCT03292809-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03292809-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 1000.0232wilson
Risk in group 20.01810.006160.0518wilson
Risk difference, group 1 minus group 2-0.0181-0.05180.00797newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one fewer participant with a serious adverse event on CyclASol Ophthalmic Solution than on Vehicle Ophthalmic Solution55.3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: vehicle.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CyclASol Ophthalmic SolutionCylclosporine A solution in vehicle~CyclASol topical ocular, eye drops: Cyclosporine A solution in vehicle0162EG000
Group 2Vehicle Ophthalmic SolutionVehicle only~Vehicle topical ocular, eye drops: Vehicle3166EG001

Harm

What it counts
Total, serious adverse events
Time frame
85 Days ± 2 (Randomization until Study Exit)

Source ClinicalTrials.gov

Trial

Title
CyclASol for the Treatment of Signs and Symptoms of Dry Eye Disease (DED)
NCT number
NCT03292809
Phases
PHASE2, PHASE3
Conditions
Dry Eye Disease
Interventions
CyclASol topical ocular, eye drops, Vehicle topical ocular, eye drops
Lead sponsor
Novaliq GmbH
Results first posted
2021-05-21

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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