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Comparison · NCT00831701-885a3d45

Tamsulosin Treatment vs Placebo Treatment: Number of Participants With Stone Expulsion

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. Tamsulosin Treatment vs Placebo Treatment: Number of Participants With Stone Expulsion. Trial comparisons, record NCT00831701-885a3d45. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00831701-885a3d45

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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 10.8670.7380.937wilson
Risk in group 20.8890.7650.952wilson
Risk difference, group 1 minus group 2-0.0222-0.1650.12newcombe hybrid score
Risk ratio, group 1 over group 20.9750.8361.14log
Odds ratio, group 1 over group 20.8130.2292.88log
Number needed to treat, for one fewer participant with the outcome on Tamsulosin Treatment than on Placebo Treatment45from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Tamsulosin TreatmentPatients received one pill of Tamsulosin 400 micrograms once daily3945OG000
Group 2Placebo TreatmentPatients received Placebo pill once daily4045OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Stone Expulsion
Description
The primary end point was the number of patients per group experiencing stone expulsion until day 21, as confirmed by low-dose abdominal computed tomography (CT).
Time frame
21 days
Population

Source ClinicalTrials.gov

Trial

Title
Medical Expulsive Therapy of Single Distal Ureteral Stones
NCT number
NCT00831701
Phases
NA
Conditions
Ureteral Calculi
Interventions
Tamsulosin, Placebo
Lead sponsor
University of Zurich
Results first posted
2010-05-12

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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