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Comparison · NCT05291598-sae

Ketorolac Group vs IV Meloxicam Group: serious adverse events

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. Ketorolac Group vs IV Meloxicam Group: serious adverse events. Trial comparisons, record NCT05291598-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05291598-sae

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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 1000.0326wilson
Risk in group 2000.034wilson
Risk difference, group 1 minus group 20-0.0340.0326newcombe 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 harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Ketorolac Group
Participants will receive the institution specific joint replacement pain protocol.~Institution specific joint replacement pain protocol: Participants will be treated with a standard orthopaedic joint replacement protocol which includes:~* Dexamethasone~* Tylenol~* Lyrica~* Celebrex~* Meloxicam~* Oxycodone~Ketorolac: Participants will be treated with ketorolac 15 mg IV push intra-operatively, followed by 15 mg IV push every 6 hours scheduled for 2 doses.
0114EG000
Group 2IV Meloxicam Group
Participants will be given IV meloxicam for pain management post total knee and hip arthroplasty.~Institution specific joint replacement pain protocol: Participants will be treated with a standard orthopaedic joint replacement protocol which includes:~* Dexamethasone~* Tylenol~* Lyrica~* Celebrex~* Meloxicam~* Oxycodone~IV meloxicam: Participants will be administered meloxicam 30 mg IV push pre-operatively.
0109EG001

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
Meloxicam for Pain Management After Total Joint Arthroplasty (TJA)
NCT number
NCT05291598
Phases
PHASE3
Conditions
Total Knee Replacement, Total Hip Replacement
Interventions
IV meloxicam, Ketorolac
Lead sponsor
University of Miami
Results first posted
2024-08-14

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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