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Randomized Sibutramine vs Randomized Placebo: Risk of Death From Any Cause (All-cause Mortality)

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.08520.07770.0933wilsonClinicalTrials.gov
Risk in group 20.08250.07510.0905wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00272-0.008270.0137newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.030.9061.18logClinicalTrials.gov
Odds ratio, group 1 over group 21.040.8981.2logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Randomized Sibutramine than on Randomized Placebo368from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Randomized Sibutramine
Subjects who completed the 6-week Lead-in Period and who were randomized and dispensed sibutramine during the Treatment Period and continued standard care for weight management. If sibutramine was prematurely discontinued, subjects continued standard care for weight management during the Follow-up Period.
4184,906OG000ClinicalTrials.gov
Group 2Randomized Placebo
Subjects who completed the 6-week Lead-in Period and who were randomized and dispensed placebo during the Treatment Period and continued standard care for weight management. If placebo was prematurely discontinued, subjects continued standard care for weight management during the Follow-up Period.
4044,898OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleRisk of Death From Any Cause (All-cause Mortality)ClinicalTrials.gov
DescriptionFor each subject who died, the time to death was evaluated using time-to-event analysis.ClinicalTrials.gov
Time frameFrom randomization up to 6 yearsClinicalTrials.gov
PopulationAnalysis based on ITT population, which consists of all randomized subjects dispensed randomized study drug and grouped according to the intervention to which they were randomized.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleA Long Term Study of Sibutramine and the Role of Obesity Management in Relation to Cardiovascular Disease in Overweight and Obese PatientsClinicalTrials.gov
NCT numberNCT00234832ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsObesityClinicalTrials.gov
InterventionsSibutramine hydrochloride, Placebo, Sibutramine hydrochlorideClinicalTrials.gov
Lead sponsorAbbottClinicalTrials.gov
Results first posted2010-04-15ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00234832?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.