ConductScience.org, home

Comparison · NCT05528588-sae

Subcutaneous Furosemide vs Oral Furosemide: 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. Subcutaneous Furosemide vs Oral Furosemide: serious adverse events. Trial comparisons, record NCT05528588-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05528588-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 10.2860.1630.451wilson
Risk in group 20.3710.2320.537wilson
Risk difference, group 1 minus group 2-0.0857-0.2910.13newcombe hybrid score
Risk ratio, group 1 over group 20.7690.391.52log
Odds ratio, group 1 over group 20.6770.2481.85log
Number needed to treat, for one fewer participant with a serious adverse event on Subcutaneous Furosemide than on Oral Furosemide11.7from 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 1Subcutaneous FurosemideThis arm received subcutaneous furosemide (n=35)1035EG000
Group 2Oral FurosemideThis group received oral furosemide.1335EG001

Harm

What it counts
Total, serious adverse events
Time frame
30 days

Source ClinicalTrials.gov

Trial

Title
Furoscix in Heart Failure Patients With Diuretic Resistance
NCT number
NCT05528588
Phases
PHASE2
Conditions
Heart Failure
Interventions
Furoscix, Diuretic Therapy
Lead sponsor
University of Texas Southwestern Medical Center
Results first posted
2025-07-16

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/NCT05528588-sae