ConductScience.org, home

Comparison · NCT01427907-sae

Calcium Acetate Oral Solution vs Sevelamer Carbonate: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Calcium Acetate Oral Solution vs Sevelamer Carbonate: serious adverse events. Trial comparisons, record NCT01427907-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01427907-sae

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.05260.01460.173wilson
Risk in group 20.02630.004660.135wilson
Risk difference, group 1 minus group 20.0263-0.08880.148newcombe hybrid score
Risk ratio, group 1 over group 220.18921.1log
Odds ratio, group 1 over group 22.060.17823.7log
Number needed to harm, for one more participant with a serious adverse event on Calcium Acetate Oral Solution than on Sevelamer Carbonate38from 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 1Calcium Acetate Oral SolutionSequence I: Calcium Acetate Oral Solution for periods 1 and 2238EG000
Group 2Sevelamer CarbonateSevelamer Carbonate for periods 1 and 2138EG001

Harm

What it counts
Total, serious adverse events
Time frame
6 months

Source ClinicalTrials.gov

Trial

Title
Equivalence of Calcium Acetate Oral Solution and Sevelamer Carbonate Tablets in Hemodialysis Patients
NCT number
NCT01427907
Phases
PHASE4
Conditions
Chronic Kidney Disease
Interventions
Calcium acetate oral solution (COS), Sevelamer carbonate
Lead sponsor
Fresenius Medical Care North America
Results first posted
2016-01-14

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT01427907-sae