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Diagnose the red baby

Fast track management of neonatal erythroderma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN12831121
Enrollment
30
Registered
2015-07-04
Start date
2014-09-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Newborn with a collodion membrane or congenital erythroderma or erythroderma developed in the first four weeks after birth. Skin and Connective Tissue Diseases

Interventions

A national multidisciplinary protocol with a diagnostic flowchart will be used. Basic diagnostics include basic laboratory investigations, a skin biopsy and 2x3 ml blood for genetic tests. The genetic

Sponsors

Erasmus Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Collodion membrane at birth or 2. Erythroderma at birth or 3. Erythroderma developed in neonatal period (first four weeks postpartum)

Exclusion criteria

Exclusion criteria: Erythroderma developed after the first month postpartum

Design outcomes

Primary

MeasureTime frame
Clinical characteristics, observed by the clinician, such as erythroderma, collodion membrane, bullae, alopecia etc. These will be measured during first clinical visit. Histological data (skin biopsy) and laboratory findings (normal blood count, total IgE, etc) will be collected. The data for these findings can be different per individual, because not every child/neonate will be seen by a clinician at the same time (e.g. day 1, week 1, etc.).

Secondary

MeasureTime frame
Morbidity and mortality

Countries

Netherlands

Outcome results

None listed

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