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Comparison · NCT03282981-c5620c62

Timolol vs SOC Plus Non Biologically Active Gel: Percentage of Complete Wound Closure, as Assessed Over a 12 Week Period

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. Timolol vs SOC Plus Non Biologically Active Gel: Percentage of Complete Wound Closure, as Assessed Over a 12 Week Period. Trial comparisons, record NCT03282981-c5620c62. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03282981-c5620c62

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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 10.3810.2080.591wilson
Risk in group 20.2590.1320.447wilson
Risk difference, group 1 minus group 20.122-0.1340.368newcombe hybrid score
Risk ratio, group 1 over group 21.470.6353.4log
Odds ratio, group 1 over group 21.760.5136.02log
Number needed to treat, for one more participant with the outcome on Timolol than on SOC Plus Non Biologically Active Gel8.22from 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 1TimololTimoptic-XE plus standard of care (SOC)~Timolol: Topical application of Timolol on non-healing diabetic foot ulcers821OG000
Group 2SOC Plus Non Biologically Active Gel
SOC plus non biologically active gel (hydrogel as placebo medication)~Non biologically active gel: Topical application of non biologically active gel (Hydrogel- standard of care) on non-healing diabetic foot ulcers
727OG001

Outcome

Type
PRIMARY
Title
Percentage of Complete Wound Closure, as Assessed Over a 12 Week Period
Description
Complete wound closure will be assessed by Investigators and is defined as 100% epithelialization of the wound site (skin re-epithelialization without drainage or dressing requirements by Week 12). The primary outcome was the proportion of patients with complete wound healing by the end of the treatment phase, evaluated using Fisher's exact test.
Time frame
12 weeks
Population
chronic, diabetic foot ulcerations

Source ClinicalTrials.gov

Trial

Title
Beta Adrenergic Antagonist for the Healing of Chronic DFU
NCT number
NCT03282981
Phases
PHASE3
Conditions
Chronic Diabetic Foot Ulcers, Diabetic Neuropathic Ulcers, Non Healing Wound
Interventions
Timolol, Non biologically active gel
Lead sponsor
VA Office of Research and Development
Results first posted
2025-04-25

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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