ConductScience.org, home

Comparison · NCT00252720-dd0274c3

Candesartan vs Placebo: Number of Participants With a Regression of Diabetic Retinopathy.

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: Number of Participants With a Regression of Diabetic Retinopathy. Trial comparisons, record NCT00252720-dd0274c3. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00252720-dd0274c3

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1470.1260.171wilson
Risk in group 20.1460.1250.17wilson
Risk difference, group 1 minus group 20.00151-0.03030.0333newcombe hybrid score
Risk ratio, group 1 over group 21.010.8131.25log
Odds ratio, group 1 over group 21.010.7851.3log
Number needed to treat, for one more participant with the outcome on Candesartan than on Placebo662from 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 daily140951OG000
Group 2PlaceboPlacebo Comparator139954OG001

Outcome

Type
SECONDARY
Title
Number of Participants With a Regression of Diabetic Retinopathy.
Description
Regression of diabetic retinopathy was defined as at least a 3 step improvement or a persistent 2-step improvement (confirmed in 2 consecutive photography sets) in the Early Treatment of Diabetic Retinopathy Study (ETDRS) severity scale. 3 steps were defined as either a 1-step change in one eye and a 2-step change in the other eye or as a 3-step change in one eye only. EDRTS is a scale with 11 steps (1-11).
Time frame
From baseline to the end of the study, i.e., 5 years
Population
The population was the Intention To Treat population which includes all randomized patients with any post-randomization data.

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-dd0274c3