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Comparison · NCT01003106-sae

BRVO vs CRVO: 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. BRVO vs CRVO: serious adverse events. Trial comparisons, record NCT01003106-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01003106-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 10.4050.270.555wilson
Risk in group 20.3080.1860.464wilson
Risk difference, group 1 minus group 20.0971-0.1090.291newcombe hybrid score
Risk ratio, group 1 over group 21.320.7242.39log
Odds ratio, group 1 over group 21.530.6113.83log
Number needed to harm, for one more participant with a serious adverse event on BRVO than on CRVO10.3from 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 1BRVOPatients with Branch Retinal Vein Occlusion1742EG000
Group 2CRVOPatients with Central Retinal Vein Occlusion1239EG001

Harm

What it counts
Total, serious adverse events
Time frame
From Baseline to Month 36

Source ClinicalTrials.gov

Trial

Title
Ranibizumab DosE Comparison and the Role of LAser in REtinal Vein Occlusions
NCT number
NCT01003106
Phases
PHASE1, PHASE2
Conditions
Retinal Vein Occlusion
Interventions
Ranibizumab 0.5mg (monthly), Ranibizumab 2.0mg (monthly), Pro re nata (prn) ranibizumab, Pro re nata (prn) Laser photocoagulation
Lead sponsor
Peter A Campochiaro, MD
Results first posted
2016-03-15

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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