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Comparison · NCT03439345-bcbd2825

Fenofibrate 145 mg vs Placebo Oral Tablet: Number of Participants With Any Progression of Diabetic Retinopathy or Maculopathy Across the NHS Scotland Retinopathy Grading Scale

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. Fenofibrate 145 mg vs Placebo Oral Tablet: Number of Participants With Any Progression of Diabetic Retinopathy or Maculopathy Across the NHS Scotland Retinopathy Grading Scale. Trial comparisons, record NCT03439345-bcbd2825. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03439345-bcbd2825

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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 10.3210.2840.36wilson
Risk in group 20.4020.3620.442wilson
Risk difference, group 1 minus group 2-0.0806-0.135-0.0251newcombe hybrid score
Risk ratio, group 1 over group 20.7990.6850.934log
Odds ratio, group 1 over group 20.7050.5530.897log
Number needed to treat, for one fewer participant with the outcome on Fenofibrate 145 mg than on Placebo Oral Tablet12.47.3939.9from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Fenofibrate 145 mgFenofibrate 145 mg: One tablet (taken daily with normal renal function, taken every second day with chronic kidney disease)185576OG000
Group 2Placebo Oral TabletPlacebo Oral Tablet: One tablet (taken daily with normal renal function, taken every second day with chronic kidney disease)231575OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Any Progression of Diabetic Retinopathy or Maculopathy Across the NHS Scotland Retinopathy Grading Scale
Description
Any progression of diabetic retinopathy or maculopathy across the NHS Scotland retinopathy grading scale. R4 = Proliferative DR, R3 = Referable background DR, R2 = Observable background DR. R1 = Mild background DR, R0 = No DR anywhere (where R4 is the highest severity grade and R0 is the lowest grade); M2 = Referable maculopathy, M1 = Observable maculopathy, M0 = No Maculopathy (where M2 is the highest severity grade and M0 is the lowest grade).
Time frame
4.0 years (interquartile range, 3.6 to 4.3) years
Population
Intention-to-treat comparisons among all randomised participants of the effects of allocation to fenofibrate versus placebo during the scheduled treatment period on time to the first occurrence

Source ClinicalTrials.gov

Trial

Title
Lowering Events in Non-proliferative Retinopathy in Scotland
NCT number
NCT03439345
Phases
PHASE4
Conditions
Diabetic Retinopathy
Interventions
Fenofibrate 145 mg, Placebo Oral Tablet
Lead sponsor
University of Oxford
Results first posted
2025-05-14

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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