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Comparison · NCT02351934-a3f608ca

Furosemide + Enhanced Recovery After Surgery (ERAS) vs Enhanced Recovery After Surgery (ERAS): Number of Participants Readmitted to Mayo Clinic Within 30-days

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. Furosemide + Enhanced Recovery After Surgery (ERAS) vs Enhanced Recovery After Surgery (ERAS): Number of Participants Readmitted to Mayo Clinic Within 30-days. Trial comparisons, record NCT02351934-a3f608ca. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02351934-a3f608ca

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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 10.210.1270.326wilson
Risk in group 20.1640.09160.276wilson
Risk difference, group 1 minus group 20.0457-0.09370.183newcombe hybrid score
Risk ratio, group 1 over group 21.280.6072.69log
Odds ratio, group 1 over group 21.350.5433.37log
Number needed to treat, for one more participant with the outcome on Furosemide + Enhanced Recovery After Surgery (ERAS) than on Enhanced Recovery After Surgery (ERAS)21.9from 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 1Furosemide + Enhanced Recovery After Surgery (ERAS)Furosemide 10 mg IV on post-operative day #1 and/or 2, plus ERAS, as described in other arm.1362OG000
Group 2Enhanced Recovery After Surgery (ERAS)
ERAS included administration of celecoxib and gabapentin in the pre-operative setting, single-injection intrathecal analgesic administration immediately prior to induction of general anesthesia, post-operative administration of scheduled acetaminophen and nonsteroidal anti-inflammatory drug (NSAID) or tramadol, and discontinuation of IV fluids by 0800 on postoperative day (POD) 1. Intraoperative fluid administration was dependent on the individual anesthesia provider with no unified commitment to either zero balance or goal-directed fluid therapy. Fluid status was determined based on patient weight. Patients were weighed preoperatively and daily post-operatively using either a bed scale or a unit-based scale.
1061OG001

Outcome

Type
SECONDARY
Title
Number of Participants Readmitted to Mayo Clinic Within 30-days
Description
Time frame
Within 30 days of release from hospital
Population
Intention to treat analysis

Source ClinicalTrials.gov

Trial

Title
Early Diuresis Following Colorectal Surgery
NCT number
NCT02351934
Phases
PHASE4
Conditions
Colorectal Disorders
Interventions
Furosemide, Celecoxib, Gabapentin
Lead sponsor
Mayo Clinic
Results first posted
2017-06-27

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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