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Comparison · NCT01029782-cb7ce747

IV Cefazolin Plus Oral Probenecid and Placebo Cephalexin vs Oral Cephalexin and Saline IV Plus Probenecid Placebo: The Number of Patients Failing Therapy After 72 Hours of Antibiotic Treatment With Oral Cephalexin or Intravenous Cefazolin Plus Oral Probenecid.

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. IV Cefazolin Plus Oral Probenecid and Placebo Cephalexin vs Oral Cephalexin and Saline IV Plus Probenecid Placebo: The Number of Patients Failing Therapy After 72 Hours of Antibiotic Treatment With Oral Cephalexin or Intravenous Cefazolin Plus Oral Probenecid. Trial comparisons, record NCT01029782-cb7ce747. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01029782-cb7ce747

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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 10.06060.02810.126wilson
Risk in group 20.04170.01630.102wilson
Risk difference, group 1 minus group 20.0189-0.04990.089newcombe hybrid score
Risk ratio, group 1 over group 21.450.4244.99log
Odds ratio, group 1 over group 21.480.4055.43log
Number needed to treat, for one more participant with the outcome on IV Cefazolin Plus Oral Probenecid and Placebo Cephalexin than on Oral Cephalexin and Saline IV Plus Probenecid Placebo52.8from 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 1IV Cefazolin Plus Oral Probenecid and Placebo CephalexinIV cefazolin plus oral probenecid and placebo cephalexin: Intravenous cefazolin 2 g IV plus probenecid 1 g daily plus cephalexin placebo orally four times daily.699OG000
Group 2Oral Cephalexin and Saline IV Plus Probenecid PlaceboOral cephalexin and saline IV plus probenecid placebo: Cephalexin 500 mg orally four times daily plus saline IV and oral probenecid placebo daily496OG001

Outcome

Type
PRIMARY
Title
The Number of Patients Failing Therapy After 72 Hours of Antibiotic Treatment With Oral Cephalexin or Intravenous Cefazolin Plus Oral Probenecid.
Description
Time frame
72 hours
Population
Per-Protocol Analysis at 72 hours.

Source ClinicalTrials.gov

Trial

Title
Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin for the Treatment of Cellulitis
NCT number
NCT01029782
Phases
PHASE2
Conditions
Cellulitis
Interventions
IV cefazolin plus oral probenecid and placebo cephalexin, Oral cephalexin and saline IV plus probenecid placebo
Lead sponsor
Kelowna General Hospital
Results first posted
2018-08-13

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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