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Comparison · NCT04588207-15a3ab3e

Urea vs No Urea: Number and Percentage of Participants Enrolled Who Completed the Study

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. Urea vs No Urea: Number and Percentage of Participants Enrolled Who Completed the Study. Trial comparisons, record NCT04588207-15a3ab3e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04588207-15a3ab3e

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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 110.3421wilson
Risk in group 210.3421wilson
Risk difference, group 1 minus group 20-0.6580.658newcombe hybrid score
Risk ratio, group 1 over group 2111log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treatfrom the risk difference intervalthe two groups' risks are equal

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1UreaNumber and percentage of participants enrolled who completed the study.22OG000
Group 2No UreaNumber and percentage of participants enrolled who completed the study.22OG001

Outcome

Type
PRIMARY
Title
Number and Percentage of Participants Enrolled Who Completed the Study
Description
Number and percentage of participants enrolled who completed the study. To be assessed by analysis of enrollment and completion data.
Time frame
9 months
Population

Source ClinicalTrials.gov

Trial

Title
Urea for Chronic Hyponatremia
NCT number
NCT04588207
Phases
PHASE2
Conditions
Hyponatremia, Inappropriate ADH Syndrome
Interventions
Urea
Lead sponsor
Helbert Rondon Berrios, MD, MS
Results first posted
2024-05-20

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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