Skip to content

Prospective evaluation of the effectiveness and life quality under UVB-311nm, UVA-1 and Blue-light in patients with atopic eczema

Prospective evaluation of the effectiveness and life quality under UVB-311nm, UVA-1 and Blue-light in patients with atopic eczema

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033975
Enrollment
150
Registered
2024-10-08
Start date
2024-07-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

L20

Interventions

Group 1: Patients suffering from atopic eczema who come to the Dermatology Department of the Bad Bentheim Specialist Clinic for an acute inpatient stay are assessed both on admission (day 1) and on di

Sponsors

Fachklinik Bad Bentheim
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis Atopic Exzema Acute inpatient stay in the dermatology department of the Bad Bentheim Specialist Clinic

Exclusion criteria

Exclusion criteria: - Exclusion of persons who are affiliated with the sponsor, study director, or the responsible physician - Exclusion of patients who, in the opinion of the medical staff providing information, are unable to accurately understand the content and significance of the study and the questionnaires and to complete them truthfully - Exclusion of patients, who are incapable of giving their informed consent

Design outcomes

Primary

MeasureTime frame
Intra-individual improvement in the level of suffering and quality of life of patients with atopic eczema under light therapy UVB-311nm, UVA-1 or Blue-Light. Assessment using the paper-based questionnaires Patient Benefit Index (PBI), to measure patient-defined treatment goals and benefits, and Dermatology Life Quality Index (DLQI) to measure quality of life, on admission (day 1) and at the end of the acute inpatient stay standard duration of 12 days (day 12).

Secondary

MeasureTime frame
Improvement in dermatological conditions under therapy and psychological well-being. Assessment using paper-based questionnaires on admission (day 1) and at the end of the acute inpatient stay with a standard duration of 12 days (day 12): Patient Health Questionnaire 9 (PHQ-9) to assess depression, Itch Controlled Days to assess the severity of itching, Generalised Anxiety Disorder 7 (GAD-7) to assess anxiety and WHO-5 to assess well-being. Assessment of the extent and intensity of eczema using the Eczema Area and Severity Index (EASI) and SCORing Atopic Dermatitis (SCORAD) scales on admission (day 1) and discharge (day 12). At discharge, additional assessment of subjective satisfaction with the light therapy UVB-311nm, UVA-1 or Blue-Light.

Countries

Germany

Contacts

Public ContactAthanasios Tsianakas

Fachklinik Bad Bentheim

a.tsianakas@fk-bentheim.de+49 5922 74 5210

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026