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Comparison · NCT00736099-cbe3c9aa

Old Lina vs New Lina: Number of Patients With Abnormalities in Clinical Chemistry: Amylase

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. Old Lina vs New Lina: Number of Patients With Abnormalities in Clinical Chemistry: Amylase. Trial comparisons, record NCT00736099-cbe3c9aa. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00736099-cbe3c9aa

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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 10.06080.04980.0739wilson
Risk in group 20.06040.04380.0829wilson
Risk difference, group 1 minus group 20.000317-0.02470.0216newcombe hybrid score
Risk ratio, group 1 over group 21.010.6891.47log
Odds ratio, group 1 over group 21.010.6731.5log
Number needed to treat, for one more participant with the outcome on Old Lina than on New Lina3,150from 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 1Old LinaPatients pre-treated with linagliptin921,514OG000
Group 2New LinaPatients pre-treated with placebo35579OG001

Outcome

Type
PRIMARY
Title
Number of Patients With Abnormalities in Clinical Chemistry: Amylase
Description
For this laboratory parameter, a possibly clinically significant abnormality is defined as a value greater than 1.5 times the upper limit of normal (ULN).
Time frame
78 weeks
Population
Treated Set with values for Amylase

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM
NCT number
NCT00736099
Phases
PHASE3
Conditions
Diabetes Mellitus, Type 2
Interventions
linagliptine 5 mg, linagliptine 5 mg and pioglitazone 30 mg
Lead sponsor
Boehringer Ingelheim
Results first posted
2012-03-08

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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