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Comparison · NCT03289351-2663e93b

2-drug Therapy vs 1-drug Therapy: Number of Participants With a Postoperative Readmission

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. 2-drug Therapy vs 1-drug Therapy: Number of Participants With a Postoperative Readmission. Trial comparisons, record NCT03289351-2663e93b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03289351-2663e93b

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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 10.1380.07850.23wilson
Risk in group 20.04880.01910.119wilson
Risk difference, group 1 minus group 20.0887-0.002820.186newcombe hybrid score
Risk ratio, group 1 over group 22.820.9368.49log
Odds ratio, group 1 over group 23.110.94610.2log
Number needed to treat, for one more participant with the outcome on 2-drug Therapy than on 1-drug Therapy11.3from 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 12-drug Therapyceftriaxone/metronidazole1180OG000
Group 21-drug Therapypiperacillin-tazobactam~Piperacillin, Tazobactam Drug Combination: Single drug therapy482OG001

Outcome

Type
SECONDARY
Title
Number of Participants With a Postoperative Readmission
Description
readmission within 30 days for any gastrointestinal complaints or infectious complications
Time frame
30 days
Population

Source ClinicalTrials.gov

Trial

Title
Two Different Antibiotics Versus One Antibiotic for Pediatric Perforated Appendicitis
NCT number
NCT03289351
Phases
PHASE4
Conditions
Perforated Appendicitis, Postoperative Infection
Interventions
Piperacillin, Tazobactam Drug Combination
Lead sponsor
Phoenix Children's Hospital
Results first posted
2024-01-12

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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