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Comparison · NCT01774604-a5eef23d

Indomethacin vs Placebo: Number of Patients With 30 Days Hospital Re-admission

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 With 30 Days Hospital Re-admission. Trial comparisons, record NCT01774604-a5eef23d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01774604-a5eef23d

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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 10.1390.09970.191wilson
Risk in group 20.08850.0580.133wilson
Risk difference, group 1 minus group 20.0505-0.008670.11newcombe hybrid score
Risk ratio, group 1 over group 21.570.9242.67log
Odds ratio, group 1 over group 21.660.9173.02log
Number needed to treat, for one more participant with the outcome on Indomethacin than on Placebo19.8from 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 131223OG000
Group 2PlaceboPlacebo suppositories (#2)~Placebo20226OG001

Outcome

Type
SECONDARY
Title
Number of Patients With 30 Days Hospital Re-admission
Description
Number of patients admitted to the hospital for any cause following ERCP
Time frame
From randomization until 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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