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Comparison · NCT01217476-sae

Trafermin 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

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ConductScience Library. Trafermin vs Placebo: serious adverse events. Trial comparisons, record NCT01217476-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01217476-sae

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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 10.190.1270.276wilson
Risk in group 20.2550.180.347wilson
Risk difference, group 1 minus group 2-0.0644-0.1770.049newcombe hybrid score
Risk ratio, group 1 over group 20.7470.4461.25log
Odds ratio, group 1 over group 20.6880.3551.33log
Number needed to treat, for one fewer participant with a serious adverse event on Trafermin than on Placebo15.5from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TraferminTrafermin 0.01% spray20105EG000
Group 2PlaceboMatching placebo spray26102EG001

Harm

What it counts
Total, serious adverse events
Time frame
Primary Treatment Emergent Adverse Event: adverse events that occurred after starting the treatment with the study medication until the end of primary follow up period up to 24 weeks.

Source ClinicalTrials.gov

Trial

Title
The TRAfermin in Neuropathic Diabetic Foot Ulcer Study - Northern Europe The TRANS-North Study
NCT number
NCT01217476
Phases
PHASE3
Conditions
Diabetic Foot Ulcer of Neuropathic Origin
Interventions
Trafermin 0.01% spray
Lead sponsor
Olympus Biotech Corporation
Results first posted
2014-08-05

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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