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Atopy Network - Comprehensive Allergy Centers: Medical Care of Patients With Moderate to Severe Allergic Diseases

Atopy Network - Comprehensive Allergy Centers: Medical Care of Patients With Moderate to Severe Allergic Diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05334940
Acronym
ATAC
Enrollment
600
Registered
2022-04-19
Start date
2022-12-08
Completion date
2025-08-31
Last updated
2024-08-21

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

Conditions

Atopic Disorders

Brief summary

The Atopy Registry aims to assess data about atopic disorders and their medical care in a standardized form. With this, the comparative efficacy, tolerability and safety of systemic therapies for atopic disorders should be investigated. An optional additional module Bioanalytic shall provide insights into further connections regarding immunology, genetics and microbiome.

Detailed description

The prevalence of atopic disorders increased in the western countries within the past decades. Atopic disorders are among others: food allergy, atopic dermatitis, allergic rhinitis, bronchial asthma, chronic spontaneous urticaria, eosinophilic esophagitis and chronic rhinosinusitis with nasal polyposis. Seriously affected patients often have coexisting atopic disorders. In fact, 60-75% of the patients with a severe atopic dermatitis also suffer from an allergic rhinoconjunctivitis and 40-50% from bronchial asthma. This leads to a decreased quality of life (LG) especially in seriously affected patients. The treatment of atopic disorders is not standardized yet. The Atopy Registry should promote the creation of a Germany-wide registry for different atopic disorders.Furthermore, the registry should characterize the medical care of patients with atopic disorders (patient satisfaction, therapy order, treatment success). This study serves as a longterm observation und is designed to compare different systemic therapies, since head-to-head studies regarding the efficacy are still missing. The analysis of biomaterial is involved to state possible correlations between endotype and phenotype.

Interventions

Patients do not receive intervention

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to No maximum

Inclusion criteria

* patients are at least 6 years old * patients with a proven moderate to severe atopic disorder who are planned to receive a biologic systemic therapy * at least one additional proven atopic disorder

Exclusion criteria

* \<2 atopic disorders * poor compliance * pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Comorbidity Food Allergy3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Food Allergy: Food Allergy Quality of Life Questionnaire (FAQLQ) (type-dependent 23-30 items, score between 0 and 6; mean of scores, minimum = 0, maximum = 6; higher score = higher impact on quality of life)
Comorbidity Atopic Dermatitis3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Atopic Dermatitis: Atopic Dermatitis-Control-Test (ADCT) (6 items, score between 0 and 4; sum, minimum = 0, maximum = 24; higher score = higher severity)
Comorbidity Bronchial Asthma3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Bronchial Asthma: Asthma-Control-Test (ACT) (5 items, score between 0 and 5; sum, minimum = 0, maximum = 25; higher score = better disease control)
Comorbidity Chronic rhinosinusitis with nasal polyps3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Chronic rhinosinusitis with nasal polyps: 22 Items Sino-Nasal Outcome Test (SNOT22) (22 items, score between 0 and 5; sum, minimum = 0, maximum = 110; higher score = higher impact on quality of life)
Comorbidity Chronic Spontaneous Urticaria3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Chronic Spointaneous Urticaria: Urticaria Control Test (UCT) (4 items, score between 0 and 5; sum, minimum = 0, maximum = 20; higher score = better control)
Comorbidity Eosinophilic Esophagitis3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Eosinophilic Esophagitis: Dysphagia Symptoms Questionnaire (DSQ) (4 items, score between 0 and 4 but question-dependent; sum, minimum = 0, maximum = 10; higher score = higher impact)
Comorbidity Allergic Rhinitis3 yearsImprovement of at least one comorbidity with biologics therapy using a standardized questionnaire to assess disease severity for the following atopic diseases: Allergic Rhinitis: Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ) (28 items, score between 0 and 6; mean, minimum = 0, maximum = 6; higher score = higher impact on quality of life)

Secondary

MeasureTime frameDescription
Chronic Spontaneous Urticaria Severity (AECT)3 yearsAltered assessment of severity using the Angioedema Control Test (AECT). (Angioedema Control Test; 4 items, score between 0 and 4; minimum = 0, maximum = 16; lower score = higher severity)
Chronic Spontaneous Urticaria Severity (UAS7)3 yearsAltered assessment of severity and/or LQ using the 7-Days Urticaria Activity Score (UAS7). (7-Days Urticaria Activity Score; 2 items on 7 days, score between 0 and 3; minimum = 0, maximum = 42; higher score = higher severity)
Food Allergy Severity3 yearsAltered assessment of severity by investigation of oral thresholds and accidental reactions by oral food challenge.
Chronic Rhinosinusitis with Nasal Polyposis Severity3 yearsAltered assessment of severity using the Nasal Polyp Score. (Nasal Polyp Score; 2 items, score between 0 and 4; minimum = 0, maximum = 8; higher score = higher severity)
Eosinophilic Esophagitis Severity and/or LQ3 yearsAltered assessment of LQ using the Pediatric Quality of Life Inventory Eosinophilic Esophagitis (PedsQLEoE). (Pediatric Quality of Life Inventory Eosinophilic Esophagitis; 33 items, score between 0 and 4; scores are graded on an 0-100 scale in opposite order (0=100, 1=75, 2=50, 3=25, 4=0); minimum = 0, maximum = 100; higher mean score = higher quality of life
Atopic Dermatitis Severity3 yearsAltered assessment of severity and/or LQ using the Eczema Area and Severity Index (EASI). (Eczema Area and Severity; minimum = 0, maximum = 72; higher numbers = higher severity)
Allergic Rhinitis Severity3 yearsAltered assessment of severity using the Total Nasal Symptom Score (TNSS). (Total Nasal Symptom Score; 3 items, score between 0 and 3; minimum = 0, maximum = 9; higher score = higher severity)
Bronchial Asthma Severity FVC3 yearsAltered assessment of severity using the lung function parameter Forced Vital Capacity (FVC)
Bronchial Asthma Severity FEV13 yearsAltered assessment of severity using the lung function parameter Forced Expiratory Volume in 1 second (FEV1)
Bronchial Asthma Severity FEF25-753 yearsAltered assessment of severity using the lung function parameter Forced expiratory flow 25-75 (FEF25-75).
Chronic Spontaneous Urticaria LQ (CUQ2oL)3 yearsAltered assessment of LQ using the Chronic Urticaria Questionnaire for Quality of Life (CUQ2oL). (Chronic Urticaria Questionnaire for Quality of Life; 23 items, score between 0 and 4; the score is calculated in percentage, minimum = 0%, maximum = 100%; higher percentage = lower quality of life)

Countries

Germany

Contacts

Primary ContactMargitta Worm, Prof.
margitta.worm@charite.de+49 30 450 518105
Backup ContactPhilipp Globig, Dr.
philipp.globig@charite.de+49 30 450 518409

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026