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Comparison · NCT02101359-sae

T2380 vs Reference Group: 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. T2380 vs Reference Group: serious adverse events. Trial comparisons, record NCT02101359-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02101359-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 10.01360.005290.0343wilson
Risk in group 20.02030.009320.0435wilson
Risk difference, group 1 minus group 2-0.00671-0.03140.0168newcombe hybrid score
Risk ratio, group 1 over group 20.6690.1912.35log
Odds ratio, group 1 over group 20.6640.1862.38log
Number needed to treat, for one fewer participant with a serious adverse event on T2380 than on Reference Group149from 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 1T2380T2380: Intracameral administration during surgery4295EG000
Group 2Reference GroupMydriatics and anesthetic: Topical treatments used the day of surgery6296EG001

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety Assessment of Intracameral Injection of T2380 in Cataract Surgery
NCT number
NCT02101359
Phases
PHASE3
Conditions
Cataract
Interventions
T2380, Mydriatics, Tetracaine
Lead sponsor
Laboratoires Thea
Results first posted
2014-09-25

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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