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Comparison · NCT00256776-sae

Thal + Dex + Velcade vs Thal + Dex: 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. Thal + Dex + Velcade vs Thal + Dex: serious adverse events. Trial comparisons, record NCT00256776-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00256776-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 10.430.3490.514wilson
Risk in group 20.3360.2610.419wilson
Risk difference, group 1 minus group 20.0938-0.02220.206newcombe hybrid score
Risk ratio, group 1 over group 21.280.9411.74log
Odds ratio, group 1 over group 21.490.9082.44log
Number needed to harm, for one more participant with a serious adverse event on Thal + Dex + Velcade than on Thal + Dex10.7from 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 1Thal + Dex + VelcadeVelcade (Bortezomib)~Thalidomide~Dexamethasone~Allocated to treatment (n=135) Received allocated treatment (n=135)58135EG000
Group 2Thal + DexStandard treatment~Thalidomide~Dexamethasone~Allocated to treatment (n=134) Received allocated treatment (n=134)45134EG001

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
MMVAR - Velcade: Study of Velcade for the Treatment of Myeloma Patients After Autologous Transplantation
NCT number
NCT00256776
Phases
PHASE3
Conditions
Multiple Myeloma
Interventions
Velcade (Bortezomib), Thalidomide, Dexamethasone
Lead sponsor
European Society for Blood and Marrow Transplantation
Results first posted
2021-10-18

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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