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Comparison · NCT05977868-066ff62a

Group 1 (Experimental) vs Group 2 (Control): Adverse Events Related to Antimicrobial Therapy

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. Group 1 (Experimental) vs Group 2 (Control): Adverse Events Related to Antimicrobial Therapy. Trial comparisons, record NCT05977868-066ff62a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05977868-066ff62a

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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 10.06450.02540.154wilson
Risk in group 20.1430.0570.315wilson
Risk difference, group 1 minus group 2-0.0783-0.2550.046newcombe hybrid score
Risk ratio, group 1 over group 20.4520.1221.68log
Odds ratio, group 1 over group 20.4140.09561.79log
Number needed to treat, for one fewer participant with the outcome on Group 1 (Experimental) than on Group 2 (Control)12.8from 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 1Group 1 (Experimental)
COpAT (oral antimicrobial therapy) on hospital discharge~Amoxicillin, amoxicillin-clavulanate, cefadroxil, cefpodoxime, cefalexin, ciprofloxacin, delafloxacin, doxycycline, levofloxacin, linezolid: COpAT (oral antimicrobial therapy) on hospital discharge
462OG000
Group 2Group 2 (Control)
Standard of care (IV antimicrobial therapy) on hospital discharge~Ampicillin, ampicillin-sulbactam, cefazolin, cefepime, ceftaroline, ceftazidime, ceftazidime-avibactam, dalbavancin, daptomycin, ertapenem: Standard of care (IV antimicrobial therapy) on hospital discharge
428OG001

Outcome

Type
PRIMARY
Title
Adverse Events Related to Antimicrobial Therapy
Description
Number of participants with adverse events requiring intervention related to antimicrobial therapy (e.g., thrombocytopenia)
Time frame
Up to 3 months after hospital discharge
Population

Source ClinicalTrials.gov

Trial

Title
Comparing Oral Versus Parenteral Antimicrobial Therapy
NCT number
NCT05977868
Phases
PHASE4
Conditions
Endovascular Infection, Bone and Joint Infection, Skin and Soft Tissue Infection, Pulmonary Infection, Gastrointestinal Infection, Genitourinary Infection
Interventions
Amoxicillin, amoxicillin-clavulanate, cefadroxil, cefpodoxime, cefalexin, ciprofloxacin, delafloxacin, doxycycline, levofloxacin, linezolid, Ampicillin, ampicillin-sulbactam, cefazolin, cefepime, ceftaroline, ceftazidime, ceftazidime-avibactam, dalbavancin, daptomycin, ertapenem
Lead sponsor
West Virginia University
Results first posted
2025-08-26

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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