At a glance
ClinicalIndex Comparison RecordN/ACompleted· 96 enrolled
Drug / intervention
Corn Foam Cushiondevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
An Open-label, Randomised, Parallel-group, No-treatment Control Investigation to Determine the Effect of the Scholl Corn Foam Cushions, on Pain Levels When Used on Heloma Durum (Hard Corns) on the Dorsal Digital (Top of the Toe) and the Plantar Weight Bearing Areas (Ball of Foot) of the Feet
In Brief
A clinical study evaluating Corn Foam Cushion for Heloma Durum. Completed, enrolled 96 participants across 1 site.
Detailed Summary
This is an open-label, single-centre, parallel-group clinical investigation to evaluate the symptomatic pain relief, consumer acceptability and in-use tolerability of the Scholl Corn Foam Cushion in participants suffering from painful Heloma Durum over a 72-hour at home in-use period compared to a no-treatment control group.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHeloma Durum
CountriesIreland
CollaboratorsO4 Research
Timeline
N/ACompletedFinished
202120222023202420252026
First PostedJan 2021
Enrollment StartJun 2021
Primary CompletionOct 2021
TodayJul 2026
First PostedJan 5, 2021
Enrollment StartJun 16, 2021
Primary CompletionOct 11, 2021
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 5.5 years ago
Interventions
Corn Foam Cushiondevice
An anatomically shaped foam pad with a central hole. The upper layer is made from a honeycomb of interconnecting cells, the external facing surface is smooth, the underside is coated with adhesive.