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Comparison · NCT01292005-dd24ffe2

Pentoxifylline vs Placebo: Number of Subjects Who Needed an Intensive Care Unit Stay

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. Pentoxifylline vs Placebo: Number of Subjects Who Needed an Intensive Care Unit Stay. Trial comparisons, record NCT01292005-dd24ffe2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01292005-dd24ffe2

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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 100.00000000000000001390.215wilson
Risk in group 20.2860.1170.546wilson
Risk difference, group 1 minus group 2-0.286-0.546-0.0123newcombe 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 fewer participant with the outcome on Pentoxifylline than on Placebo3.51.8381.2from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PentoxifyllinePentoxifylline, 400 mg, 3 times daily by mouth from time of enrollment until 72 hours from enrollment. Subjects received up to a maximum of 9 doses.014OG000
Group 2PlaceboPlacebo, 400 mg, 3 times daily by mouth from time of enrollment until 72 hours from enrollment. Subjects received up to a maximum of 9 doses.414OG001

Outcome

Type
SECONDARY
Title
Number of Subjects Who Needed an Intensive Care Unit Stay
Description
Time frame
30 days, or until dismissal, whichever came first
Population

Source ClinicalTrials.gov

Trial

Title
Pentoxifylline Treatment of Acute Pancreatitis
NCT number
NCT01292005
Phases
EARLY_PHASE1
Conditions
Acute Pancreatitis
Interventions
Pentoxifylline, Placebo
Lead sponsor
Mayo Clinic
Results first posted
2013-12-13

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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