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Comparison · NCT00004635-51957644

Thalidomide vs Placebo: The Number of Participants With 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. Thalidomide vs Placebo: The Number of Participants With Adverse Events. Trial comparisons, record NCT00004635-51957644. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00004635-51957644

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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 10.8480.7790.898wilson
Risk in group 20.790.710.853wilson
Risk difference, group 1 minus group 20.0575-0.03570.152newcombe hybrid score
Risk ratio, group 1 over group 21.070.9561.2log
Odds ratio, group 1 over group 21.480.7842.79log
Number needed to treat, for one more participant with the outcome on Thalidomide than on Placebo17.4from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1ThalidomideParticipants who received thalidomide in period 1 or 2.117138OG000
Group 2PlaceboParticipants who received placebo in period 1 or 2.98124OG001

Outcome

Type
SECONDARY
Title
The Number of Participants With Adverse Events
Description
Here are the total number of participants with adverse events. For the detailed list of adverse events see the adverse event module.
Time frame
Date treatment consent signed to date off study, approximately 60 months
Population

Source ClinicalTrials.gov

Trial

Title
Thalidomide for the Treatment of Hormone-Dependent Prostate Cancer
NCT number
NCT00004635
Phases
PHASE3
Conditions
Prostate Cancer
Interventions
Thalidomide, leuprolide acetate, goserelin, Placebo
Lead sponsor
National Cancer Institute (NCI)
Results first posted
2012-09-12

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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