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Comparison · NCT06053541-deaths

Tiotropium Treatment - MAT1 vs Glycopyrronium Treatment - MAT2: 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. Tiotropium Treatment - MAT1 vs Glycopyrronium Treatment - MAT2: deaths from any cause. Trial comparisons, record NCT06053541-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT06053541-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 10.07820.06010.101wilson
Risk in group 20.08760.06960.11wilson
Risk difference, group 1 minus group 2-0.00939-0.0380.0198newcombe hybrid score
Risk ratio, group 1 over group 20.8930.6311.26log
Odds ratio, group 1 over group 20.8840.6051.29log
Number needed to treat, for one fewer death from any cause on Tiotropium Treatment - MAT1 than on Glycopyrronium Treatment - MAT2107from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Tiotropium Treatment - MAT1
In the MAT1 (total arithmetic mean 1) period, August 2017 to July 2018 data cut available in the DATASUS (Unified Health Brazilian System Informatics Department (in Portuguese)), patients received Tiotropium bromide in soft mist inhaler (SPIRIVA® RESPIMAT®) as part of the treatment plan for Chronic Obstructive Pulmonary Disease (COPD) defined by the Health State Secretariat of Distrito Federal (DF) in Brazil.
52665EG000
Group 2Glycopyrronium Treatment - MAT2
In the MAT2 (total arithmetic mean 2) period, August 2018 to July 2019 data cut available in the DATASUS (Unified Health Brazilian System Informatics Department (in Portuguese), patients received Glycopyrronium bromide in dry powder inhaler (Seebri® Breezhaler®) as part of the treatment plan for Chronic Obstructive Pulmonary Disease (COPD) defined by the Health State Secretariat of Distrito Federal (DF) in Brazil.
67765EG001

Harm

What it counts
Total, all-cause mortality
Time frame

Source ClinicalTrials.gov

Trial

Title
Morbid Rates After Spiriva Chronic Obstructive Pulmonary Disease (COPD) Protocol Change
NCT number
NCT06053541
Phases
Conditions
Pulmonary Disease, Chronic Obstructive
Interventions
Lead sponsor
Boehringer Ingelheim
Results first posted
2024-10-26

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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