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Comparison · NCT03607838-deaths

SI-6603 vs Sham: deaths from any cause

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. SI-6603 vs Sham: deaths from any cause. Trial comparisons, record NCT03607838-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03607838-deaths

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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 10.005990.001060.0331wilson
Risk in group 2000.0216wilson
Risk difference, group 1 minus group 20.00599-0.01620.0331newcombe 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 harm, for one more death from any cause on SI-6603 than on Sham167from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: sham.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1SI-6603Condoliase: 1.25U, intradiscal injection, one time~For patients in the active treatment group, a volume of 1.0 mL was administered into the intervertebral disc in a single dose.1167EG000
Group 2ShamSham injection~For patients in the control group, a solution was not prepared, and the needle was not placed in the intervertebral disc.0174EG001

Harm

What it counts
Total, all-cause mortality
Time frame
52 weeks

Source ClinicalTrials.gov

Trial

Title
SI-6603 (Condoliase) Study for Lumbar Disc Herniation (Discovery 6603 Study)
NCT number
NCT03607838
Phases
PHASE3
Conditions
Lumbar Disc Herniation
Interventions
SI-6603, Sham injection
Lead sponsor
Seikagaku Corporation
Results first posted
2025-07-11

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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