ConductScience.org, home

Comparison · NCT00252720-sae

Candesartan vs Placebo: 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. Candesartan vs Placebo: serious adverse events. Trial comparisons, record NCT00252720-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00252720-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 10.1820.1590.208wilson
Risk in group 20.1690.1470.194wilson
Risk difference, group 1 minus group 20.0126-0.02160.0468newcombe hybrid score
Risk ratio, group 1 over group 21.070.8841.31log
Odds ratio, group 1 over group 21.090.8611.38log
Number needed to harm, for one more participant with a serious adverse event on Candesartan than on Placebo79.2from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CandesartanCandesartan cilexetil 32 mg once daily173951EG000
Group 2PlaceboPlacebo Comparator161951EG001

Harm

What it counts
Total, serious adverse events
Time frame
During treatment. During Treatment refers to the period of actual treatment with randomized study drug, ie, is a subset of the patients included in During Study. During Treatment period only includes AEs reported while patients were on study treatment.

Source ClinicalTrials.gov

Trial

Title
DIabetic Retinopathy Candesartan Trials.
NCT number
NCT00252720
Phases
PHASE3
Conditions
Type 1 Diabetes
Interventions
candesartan
Lead sponsor
AstraZeneca
Results first posted
2014-06-03

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/NCT00252720-sae