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NCT Number: NCT06035289

Register Schweres Asthma - German Asthma Net e.V.

The German Asthma Net e.V. focusses on science and research in patients with severe asthma. This includes, in particular, the optimization of medical care and treatment for patients with severe asthma as well as the elucidation and information. An unavoidable basis for a better understanding of severe asthma is the registration and comprehensive characterization of a large patient population. To date, there are only few reliable data on incidence, prevalence, phenotypes and treatment of patients with severe asthma. For this reason, the German Asthma Net e.V. was established in December 2011 as a clinical registry for patients with severe asthma, initially set up on a national basis.

Recruiting

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Key information

Age range

6 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Kardiologische und fachinternistische ÜBAG Dr. Sandrock und Partner, Altdorf, Germany

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About this study

Sociodemographic parameters (e.g., gender, date of birth) and medical parameters (diagnosis, therapy) are entered in the register. In addition, data on lung function, laboratory values (IgE and eosinophil granulocytes), asthma control (symptoms, nocturnal awakenings, on-demand medication, exacerbations), smoking status, and concomitant therapy (inhalable corticosteroids, bronchodilators, and systemic steroids) are collected. This information will be collected at the baseline visit, and then once a year at a follow up visit, for fifteen years.

Participants will be assigned a unique study ID to protect the confidentiality of their personal health care information. Personal data and register data are on separate servers and thus meet the requirements of data protection.

The primary purpose is to establish a clinical registry for patients with severe asthma. The number of patients with severe asthma at a single center or practice is usually small, so several centers (clinics and practices) in Germany have joined together to form the German Asthma Net e.V. to optimize the diagnostic evaluation and treatment of patients with severe asthma.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Definition: Severe asthma in children and adolescents

Poor symptom control in the last year despite (medium to) high doses of anti-inflammatory maintenance treatment:

(i) Age 6-18 years (at inclusion) (ii) Asthma diagnosis made by a medical doctor (iii) Potential differential diagnoses excluded (iv) Good compliance and trained inhalation technique (v) Evidence of:

a. Positive bronchodilator reversibility testing (≥ 12% increase in FEV1 after SABA) or b. Significant bronchial hyperreactivity (BHR) after unspecific provocation test (e.g. methacholine challenge or treadmill) according to ATS criteria (Am J Respir Crit Care Med 2000) (vi) High level of treatment:

  • Maintenance treatment with high doses of ICS (>400 μg budesonide or equivalent / ≥ 200 μg of fluticasone as monotherapy) or
  • Maintenance treatment with medium to high doses of ICS (≥400 μg budesonide or equivalent / ≥ 200 μg fluticasone) combined with LABA and/or LTRA and/or theophylline or
  • Treatment with oral steroids for ≥ 3 months (vii) Poor asthma control:

a. Inadequate symptom in the past 4 weeks: i. asthma symptoms ≥3 x / week or use of rescue medication ≥3 x / week; or ii. activity limitations due to asthma; or iii. any nighttime asthma symptoms; or b. ≥ 1 exacerbation in the last year with ≥ 3 days of OCS treatment or hospitalisation or b. Poor lung function with reduced Tiffeneau index or FEV1 at inclusion (viii) written informed consent (parent or legal guardian)

Exclusion criteria

(i) Diagnosis of other obstructive or systemic pulmonary diseases (e.g. cystic fibrosis, COPD) despite BPD at inclusion (ii) Other congenital lung diseases or pulmonary malformations (iii) Other significant chronic diseases (iv) Congenital or acquired heart defects with significant functional limitations

Definition: Severe asthma in adults

High level of treatment (A), i.e. step 5 of GINA guideline or (B) medium level of treatment and poor symptom control:

(A) High level of treatment:

  • Maintenance treatment with high-dose inhaled corticosteroids (≥ 1000 μg beclomethasone (BDP, powder) or equivalent) in combination with LABA or LTRA or theophylline or
  • Maintenance treatment with oral corticosteroids (OCS) for ≥3 months independent of other asthma treatments or
  • Treatment with monoclonal antibodies independent of other asthma treatments

B) Medium level of treatment and poor symptom control:

  • Maintenance treatment with medium to high doses of ICS (≥ 500 μg BDP (powder) or equivalent) in combination with LABA or LTRA or theophylline and
  • Poor symptom control:

(i) asthma symptoms ≥ 3 x / week or use of rescue medication ≥ 3 x / week; or (ii) activities limited due to asthma; or (iii) any nighttime asthma symptoms; or (iv) ≥ 1 exacerbation in the last year with ≥ 3 days of OCS treatment or (v) FEV1<80% of predicted

Treatment and study plan

Primary outcomes

  1. Symptom Control

    Time frame: Baseline, four months, yearly for up to 15 years

    Changes in symptom control at baseline and during the follow-up period and at study end using the Asthma Control Test (ACT).

Secondary outcomes

  1. Exacerbations

    Time frame: Baseline, four months, yearly for up to 15 years

    Number of exacerbation with/without hospitalization

  2. Utilization of the health care system

    Time frame: Baseline, yearly for up to 15 years

    Number of visits at a pneumologist/ specialist, number of emergency consultations, number of hospitalizations, number of rehabilitation stays

  3. Symptoms and health-related quality of life

    Time frame: Baseline, yearly for up to 15 years

    Asthma Control Test (ACT: 5 questions, scale 1- 5, min score 5, max score 25, the lower the score the better the Asthma control)

  4. Quality of Life Questionnaire

    Time frame: Baseline, yearly for up to 15 years

    Mini Asthma Quality of Life Questionnaire (Mini-AQLQ: 15 questions, scale 1 to 7, min score 15, max score 105, the higher the score, the better the quality of life)

  5. Asthma Control Questionnaire

    Time frame: Baseline, yearly for up to 15 years

    Asthma Control Questionnaire ACQ: 5 questions, scale 0 to 6, min score 0, max score 30, the lower the score the better the Asthma control)

  6. Forced Exhaled Volume in 1 second (FEV1)

    Time frame: Baseline, 4 months, yearly for up to 15 years

    FEV1 at consultation, FEV1 last 2 years, changes in FEV1 in liter from the target value

  7. Forced Vital Capacity (FVC)

    Time frame: Baseline, 4 months, yearly for up to 15 years

    FVC at consultation, FEV1 last 2 years, changes in FEV1 in liter from the target value

  8. Changes in medication

    Time frame: Baseline, 4 months, yearly for up to 15 years

    changes in substances if there is a new drug used.

  9. Changes in dose in mg

    Time frame: 4 months, yearly for up to 15 years

    Changes in dose in mg

  10. Fraction of exhaled nitric oxide (FeNo)

    Time frame: Baseline, 4 months, yearly for up to 15 years

    Changes in FeNo in ppb

  11. Blood Gas analysis

    Time frame: Baseline, 4 months, yearly for up to 15 years

    pO2 in kPa/ mmHg, pCO2 in kPa/ mmHg

  12. Blood Gas analysis

    Time frame: Baseline, 4 months, yearly for up to 15 years

    Blood-oxygen saturation in %

  13. Leucocytes

    Time frame: Baseline, 4 months, yearly for up to 15 years

    Changes in leucocytes in nl

  14. Neutrophilic granulocytes

    Time frame: Baseline, 4 months, yearly for up to 15 years

    Changes in Neutrophilic granulocytes in nl or %

  15. Eosinophilic granulocytes

    Time frame: Baseline, 4 months, yearly for up to 15 years

    Changes in Eosinophilic granulocytes in µl or %

  16. CO diffusion capacity

    Time frame: Baseline, yearly for up to 15 years

    Changes in mmol/min/kPa/ %

Study contacts

Contact information is provided by the study sponsor or research team.

Mandy Seefeldt

CONTACT

[email protected]

+49 (0)1577-6948673

Stephanie Korn, Prof.

CONTACT

[email protected]

+49 (0)1577-6948673

Sponsors and collaborators

Lead sponsor

German Asthma Net e.V.

Other

Collaborators

  • AstraZeneca
  • Chiesi Farmaceutici S.p.A.
  • GlaxoSmithKline
  • Sanofi

Registry information

Official study title

Klinisches Register Schweres Asthma

Important dates

Study start
2011
Primary completion
2026
Study completion
2026
First posted
Sep 13, 2023
Registry last updated
Oct 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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