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Comparison · NCT03587142-deaths

Buspirone vs Placebo: 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. Buspirone vs Placebo: deaths from any cause. Trial comparisons, record NCT03587142-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03587142-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 1000.0756wilson
Risk in group 200.000000000000000006940.0727wilson
Risk difference, group 1 minus group 20-0.07270.0756newcombe 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 harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1BuspironeBuspirone HCl 10 mg capsule orally three times daily, 30 minutes before each meal, for 4-weeks~Buspirone: Buspirone tablet047EG000
Group 2PlaceboPlacebo capsule orally three times daily, 30 minutes before each meal, for 4-weeks; manufactured to look identical to buspirone capsule~Placebo: Sugar pill manufactured to mimic buspirone 10 mg tablet049EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events were counted after randomization through end of treatment at 4-weeks.

Source ClinicalTrials.gov

Trial

Title
Buspirone for Early Satiety and Symptoms of Gastroparesis
NCT number
NCT03587142
Phases
PHASE2
Conditions
Gastroparesis
Interventions
Buspirone, Placebo
Lead sponsor
Johns Hopkins Bloomberg School of Public Health
Results first posted
2023-06-15

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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