Ludvigsen 1975.
Study characteristics | |
Methods | Trial design: randomised, double‐blind, within‐participant study Trial registration number: not reported Country: Denmark Outpatient or hospital, date trial conducted: not reported Duration of trial participation: 14 days Inclusion criteria: AD with similar lesions Exclusion criteria: not reported Additional design details: none |
Participants | Total number randomised: 50 participants (50 sides to apply the intervention and 50 sides to apply the comparator) Age: range from 6 months to 22 years Sex, ethnicity, duration of eczema, severity of eczema, body site: not reported Number of withdrawals: 4 did not attend follow‐up; reason why not provided Notes: none |
Interventions | Run‐in details: not reported Intervention: calmuril‐hydrocortisone 1% cream used twice daily for "approx" 14 days · Concurrent treatment: not reported · Other key information: none Comparator: triamcinolone acetonide 0.1% cream used twice daily for "approx" 14 days · Concurrent treatment: not reported · Other key information: none Concurrent treatments received alongside both intervention and comparator: not reported Notes: none |
Outcomes | · to quote: "morphological exemplification changes" · Itch · Dryness · Patient preference · AE |
Notes | Funding source: not reported Declarations of interest: not declared Original language of publication: Danish Other: Paper in Danish. Translation via google translation and google app, plus advice of native Danish speaker on results |