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. 2024 Aug 6;2024(8):CD015064. doi: 10.1002/14651858.CD015064.pub2

Gutgesell 1998.

Methods Trial design: double‐blind, within‐participant study
Trial registration number, country, outpatient or hospital, date trial conducted, duration of trial participation: not reported
Inclusion criteria: adults with severe longstanding AD
Exclusion criteria: not reported
Additional design details: study awaiting classification as unclear if randomised
Participants Total number randomised: number reported but not clear if randomised
Age: 22 to 36 years
Sex, ethnicity, duration of eczema, severity of eczema, body site, number of withdrawals: not reported
Notes: none
Interventions Run‐in details: not reported
Intervention: tacrolimus 0.1% ointment used once or twice daily for 21 days
· Concurrent treatment: not reported
· Other key information: none
Comparator: hydrocortisone 3.% ointment used once or twice daily for 21 days
· Concurrent treatment: not reported
· Other key information: none
Concurrent treatments received alongside both intervention and comparator: the area of treatment did not exceed 20% of the whole BSA.
Notes: none
Outcomes · Modified SCORAD
· Pruritus
· AE
Notes Funding source: not reported
Declarations of interest: not declared
Original language of publication: English
Other: unclear study design (abstract only)