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Comparison · NCT01774604-2f8d2278

Indomethacin vs Placebo: Number of Patients Who Developed Moderately Severe Pancreatitis

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. Indomethacin vs Placebo: Number of Patients Who Developed Moderately Severe Pancreatitis. Trial comparisons, record NCT01774604-2f8d2278. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01774604-2f8d2278

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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 1000.0169wilson
Risk in group 20.004420.0007820.0246wilson
Risk difference, group 1 minus group 2-0.00442-0.02460.0129newcombe 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 Indomethacin than on Placebo226from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1IndomethacinIndomethacin 100 mg PR x 1 in peri-procedural period~Indomethacin: 100 mg Indomethacin PR x 10223OG000
Group 2PlaceboPlacebo suppositories (#2)~Placebo1226OG001

Outcome

Type
SECONDARY
Title
Number of Patients Who Developed Moderately Severe Pancreatitis
Description
Number of patients with moderately severe pancreatitis based on Atlanta Classification
Time frame
From randomization to 30 days after ERCP
Population

Source ClinicalTrials.gov

Trial

Title
Rectal Indomethacin to Prevent Post-Endoscopic Retrograde Cholangiopancreatography (ERCP) Pancreatitis
NCT number
NCT01774604
Phases
PHASE3
Conditions
Post-ERCP Acute Pancreatitis
Interventions
Indomethacin, Placebo
Lead sponsor
Dartmouth-Hitchcock Medical Center
Results first posted
2016-09-20

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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