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Comparison · NCT01226706-aba9e56e

Botulinum Toxin Type A vs Placebo: Frequency of Participants Needing Self-catheterization From Baseline to 6 Month Follow-up

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. Botulinum Toxin Type A vs Placebo: Frequency of Participants Needing Self-catheterization From Baseline to 6 Month Follow-up. Trial comparisons, record NCT01226706-aba9e56e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01226706-aba9e56e

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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 10.09090.01620.377wilson
Risk in group 2000.278wilson
Risk difference, group 1 minus group 20.0909-0.1960.377newcombe 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 treat, for one more participant with the outcome on Botulinum Toxin Type A than on Placebo11from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Botulinum Toxin Type ABotulinum toxin Type A 100U injected into the detrusor at Day 1~botulinum toxin Type A: Botulinum toxin Type A 100U injected into the detrusor at Day 1111OG001
Group 2Placebo
Placebo injected into the detrusor at Day 1,~Placebo: Placebo injected into the detrusor at Day 1, followed by injection of botulinum toxin Type A 100U after 24 weeks has elapsed from previous treatment, if requested/qualified.
010OG000

Outcome

Type
SECONDARY
Title
Frequency of Participants Needing Self-catheterization From Baseline to 6 Month Follow-up
Description
Frequency of participants needing self-catheterization from baseline to 6 month follow-up.
Time frame
Baseline to 6 months
Population

Source ClinicalTrials.gov

Trial

Title
Efficacy of Botulinum Toxin Type A for the Treatment of Non-neurogenic Urinary Urge Incontinence
NCT number
NCT01226706
Phases
NA
Conditions
Urinary Urge Incontinence
Interventions
Botulinum Toxins, Type A, Placebos
Lead sponsor
Saskatchewan Health Authority - Regina Area
Results first posted
2017-07-03

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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