Comparison · NCT02787057-d2477ca2
Study Group vs Control Group: Primary Response Rate
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Study Group vs Control Group: Primary Response Rate. Trial comparisons, record NCT02787057-d2477ca2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02787057-d2477ca2
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.675 | 0.52 | 0.799 | wilson | |
| Risk in group 2 | 0.8 | 0.652 | 0.895 | wilson | |
| Risk difference, group 1 minus group 2 | -0.125 | -0.307 | 0.0679 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.844 | 0.647 | 1.1 | log | |
| Odds ratio, group 1 over group 2 | 0.519 | 0.187 | 1.44 | log | |
| Number needed to treat, for one fewer participant with the outcome on Study Group than on Control Group | 8 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: control.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Study Group | IP vancomycin 1g every 5 days combined with oral moxifloxacin 400mg QD. The duration of treatment was based on ISPD guideline recommendations.~vancomycin: IP vancomycin 1g every 5 days~moxifloxacin: oral moxifloxacin 400mg QD | 27 | 40 | OG001 |
| Group 2 | Control Group | IP vancomycin 1g every 5 days combined with IP ceftazidime 1g QD. The duration of treatment was based on internatinal society of peritoneal dialysis (ISPD) guideline recommendations.~vancomycin: IP vancomycin 1g every 5 days~ceftazidime: IP ceftazidime 1g QD | 32 | 40 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Primary Response Rate
- Description
Primary response was defined as resolution of peritonitis (normalization of body temperature, resolution of abdominal pain, clearing of dialysate, and PD effluent neutrophil count less than 100 cells/mL and proportion of polynuclear cell less than 50%) on day 10 by using antibiotics alone
- Time frame
- on day 10 by using antibiotics alone
- Population
Source ClinicalTrials.gov
Trial
- Title
- Vancomycin Plus Moxifloxacin Versus Vancomycin Plus Ceftazidime for the Treatment of Peritoneal Dialysis (PD)-Related Peritonitis
- NCT number
- NCT02787057
- Phases
- NA
- Conditions
- Peritoneal Dialysis Associated Peritonitis
- Interventions
- vancomycin, moxifloxacin, ceftazidime
- Lead sponsor
- Peking University First Hospital
- Results first posted
- 2020-03-26
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02787057?tab=results
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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