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Comparison · NCT01654536-b89274fa

Ciclesonide Nasal Aerosol vs Ciclesonide Nasal Spray: Number of Subjects With Development of or Worsening in Lens Opacities.

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. Ciclesonide Nasal Aerosol vs Ciclesonide Nasal Spray: Number of Subjects With Development of or Worsening in Lens Opacities. Trial comparisons, record NCT01654536-b89274fa. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01654536-b89274fa

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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 10.1390.1070.178wilson
Risk in group 20.1430.1110.183wilson
Risk difference, group 1 minus group 2-0.00428-0.05480.0463newcombe hybrid score
Risk ratio, group 1 over group 20.970.6791.39log
Odds ratio, group 1 over group 20.9650.6381.46log
Number needed to treat, for one fewer participant with the outcome on Ciclesonide Nasal Aerosol than on Ciclesonide Nasal Spray234from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Ciclesonide Nasal AerosolZetonna (ciclesonide) nasal aerosol 74 mcg~ciclesonide nasal aerosol: ciclesonide nasal aerosol 74 mcg (given as 1 actuation per nostril of 37 mcg ciclesonide nasal aerosol)51367OG000
Group 2Ciclesonide Nasal SprayOmnaris (ciclesonide) nasal spray 200 mcg~ciclesonide nasal spray: ciclesonide nasal spray 200 mcg (given as 2 actuations per nostril of 50 mcg ciclesonide nasal spray)53370OG001

Outcome

Type
SECONDARY
Title
Number of Subjects With Development of or Worsening in Lens Opacities.
Description
Time frame
0-6 months
Population

Source ClinicalTrials.gov

Trial

Title
A 6 Month Safety Study Of Ciclesonide Nasal Aerosol (Zetonna®) And Ciclesonide Nasal Spray (Omnaris®) In Subjects 12 Years And Older With Perennial Allergic Rhinitis (PAR)
NCT number
NCT01654536
Phases
PHASE4
Conditions
Perennial Allergic Rhinitis
Interventions
ciclesonide nasal aerosol, ciclesonide nasal spray
Lead sponsor
Sumitomo Pharma America, Inc.
Results first posted
2014-07-24

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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