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Clinical Trials in France / NCT07280091
Recruiting Observational

Study of Skin and Gut Microbiome in a Skin Condition Involving Skin Barrier Impairment and Allergic Symptoms: Netherton Syndrome

NCT07280091 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-05-26
Last updated
2026-06-30

Condition(s) studied

Netherton Syndrome

Investigational drug(s) / intervention(s)

Superficial skin swabsSuperficial skin swabsStool samples →Saliva samples →Blood samples →Blood samples →Data-CollectionData-Collection

Superficial skin swabs: Sampling areas: (18 swabs in total + 6 swabs for routine skin mapping) 1. Lesion area outside skin folds (e.g., back or limb) 2. Healthy area outside skin folds (e.g., back or limb) 3. Perioral area of the face 4. Scalp 5. Inguinal fold 6. Axillary fold

Superficial skin swabs: Three superficial skin swabs: same locations as for Netherton patients

Stool samples: A stool sample collected for analysis of the fecal microbiome and mycobiome.

Saliva samples: A saliva sample collected for analysis of the saliva microbiome and mycobiome.

Blood samples: For group A: cytokine profile from an additional blood sample taken during a blood draw for treatment For group B: cytokine profile if there is any residual blood sample from the treatment

Blood samples: For group A: cytokine profile from an additional blood sample taken during a blood draw for treatment For group B: cytokine profile if there is any residual blood sample from the treatment

Data-Collection: Socio-demographic data and lifestyle habits of the patient and parents

Data-Collection: Clinical data, treatment data, and results of biological tests carried out as part of routine monitoring

Study summary

It is proposed to conduct an exploratory study to analyze the skin, intestinal, and salivary microbiome, as well as the skin mycobiome and virome, of patients (adolescents and young adults) with Netherton syndrome, a condition characterized by an impaired skin barrier that most likely promotes the development of allergic manifestations.

The study will be conducted on patients with Netherton syndrome and control subjects in order to investigate possible correlation factors between the three microbiomes and identify which ones.

Eligibility

Sex
ALL
Min age
10 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Group A: * Children aged 10 years and older and adults with confirmed Netherton syndrome diagnosed at age 10 years or older (clinical and histological and/or molecular) * Patients and legal guardians informed about the study and not opposed to participation in the study Group B: * Children aged 10 years and older and adults with no skin barrier impairment, dermatosis, inflammatory disease, or autoimmune disease. * Subjects and legal guardians informed about the study and who do not object to participation in the study. Exclusion Criteria: * Refusal by parents/guardians, children, adolescents, or adults. * General or local antibiotic therapy within the month preceding the consultation.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hôpital Necker Enfants Malades Paris Île-de-France Region Recruiting

More Assistance Publique - Hôpitaux de Paris trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07280091 on ClinicalTrials.gov ↗ ← All trials in France