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Comparison · NCT00660530-sae

Chewed Lanthanum Carbonate vs Crushed Lanthanum 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

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ConductScience Library. Chewed Lanthanum Carbonate vs Crushed Lanthanum Carbonate: serious adverse events. Trial comparisons, record NCT00660530-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00660530-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 10.09090.01620.377wilson
Risk in group 20.1820.05140.477wilson
Risk difference, group 1 minus group 2-0.0909-0.3950.224newcombe hybrid score
Risk ratio, group 1 over group 20.50.05274.75log
Odds ratio, group 1 over group 20.450.03475.84log
Number needed to treat, for one fewer participant with a serious adverse event on Chewed Lanthanum Carbonate than on Crushed Lanthanum Carbonate11from 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 1Chewed Lanthanum CarbonateLanthanum carbonate 1 g to be chewed, three times daily with meals111EG000
Group 2Crushed Lanthanum CarbonateLanthanum carbonate 1 g crushed into a fine powder, three times daily with meal211EG001

Harm

What it counts
Total, serious adverse events
Time frame
4 weeks for each cross-over period

Source ClinicalTrials.gov

Trial

Title
Chewed vs. Crushed Lanthanum Carbonate in Hemodialysis Patients
NCT number
NCT00660530
Phases
PHASE2
Conditions
Hyperphosphatemia, Kidney Disease
Interventions
Lanthanum Carbonate Chewable Product, Lanthanum carbonate crushed powder
Lead sponsor
University of Illinois Chicago
Results first posted
2020-10-01

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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GET https://conductscience.org/api/comparisons/v1/NCT00660530-sae