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Comparison · NCT01189890-8a3b4be6

Sitagliptin vs Glimepiride: Number of Participants With an Adverse Event of Symptomatic Hypoglycemia Up to Week 30

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. Sitagliptin vs Glimepiride: Number of Participants With an Adverse Event of Symptomatic Hypoglycemia Up to Week 30. Trial comparisons, record NCT01189890-8a3b4be6. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01189890-8a3b4be6

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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 10.00830.002280.0297wilson
Risk in group 20.04660.02620.0815wilson
Risk difference, group 1 minus group 2-0.0383-0.0737-0.00872newcombe hybrid score
Risk ratio, group 1 over group 20.1780.03990.795log
Odds ratio, group 1 over group 20.1710.03750.781log
Number needed to treat, for one fewer participant with the outcome on Sitagliptin than on Glimepiride26.113.6115from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1SitagliptinSitagliptin phosphate 100 mg once daily (QD) or 50 mg QD2241OG000
Group 2GlimepirideGlimepiride 1-6 mg QD11236OG001

Outcome

Type
PRIMARY
Title
Number of Participants With an Adverse Event of Symptomatic Hypoglycemia Up to Week 30
Description
Symptomatic hypoglycemia was defined as an episode with clinical symptoms attributed to hypoglycemia, without regard to glucose level. Participants were instructed to complete the Hypoglycemia Assessment Log (HAL) for any symptomatic episodes he or she believed represent hypoglycemia. If a fingerstick glucose was obtained before or shortly (i.e., within a few minutes) after treating, the value was recorded in the HAL. In addition, participants were instructed to record in the HAL any fingerstick glucose values ≤70 mg/dL (≤3.9 mmol/L) regardless of the presence of clinical symptoms.
Time frame
Up to Week 30
Population
All randomized participants who received at least one dose of study treatment.

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Sitagliptin Compared With Glimepiride in Elderly Participants With Type 2 Diabetes Mellitus (MK-0431-251)
NCT number
NCT01189890
Phases
PHASE3
Conditions
Type 2 Diabetes Mellitus
Interventions
sitagliptin phosphate, Glimepiride, Placebo to Sitagliptin, Placebo to Glimepiride
Lead sponsor
Merck Sharp & Dohme LLC
Results first posted
2013-06-27

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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