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Comparison · NCT02874144-sae

AZ+INCS vs Placebo + INCS: 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. AZ+INCS vs Placebo + INCS: serious adverse events. Trial comparisons, record NCT02874144-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02874144-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 10.04550.008070.218wilson
Risk in group 20.04760.008460.227wilson
Risk difference, group 1 minus group 2-0.00216-0.1850.175newcombe hybrid score
Risk ratio, group 1 over group 20.9550.063714.3log
Odds ratio, group 1 over group 20.9520.055716.3log
Number needed to treat, for one fewer participant with a serious adverse event on AZ+INCS than on Placebo + INCS462from 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 1AZ+INCSAZD1981 40 mg three times a day , added to 2 sprays daily of intranasal corticosteroid (INCS) spray for 12 weeks.122EG000
Group 2Placebo + INCSMatched Placebo (1:1 randomization) three times a day added to 2 sprays daily of intranasal corticosteroid (INCS) spray for 12 weeks121EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse Events were assessed every 2 weeks for the first month, then every 4 weeks for 12 weeks and during a 4 week washout period, an average of 5 months.

Source ClinicalTrials.gov

Trial

Title
Anti-Inflammatory Agent in Sinusitis
NCT number
NCT02874144
Phases
PHASE2
Conditions
Nasal Polyps
Interventions
AZ compound, Collection of Biological Specimens, Intranasal corticosteroid, Placebo
Lead sponsor
Northwestern University
Results first posted
2022-05-25

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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