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The German National CRS Registry (GenreCRS): Clinical Evaluation of the New European Academy for Allergy and Clinical Immunology (EAACI) Criteria for CRSwNP Disease Control, Remission and Cure in a Real-World Evidence Study Approach

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Ärzteverband Deutscher Allergologen e.V.

Status

Not yet enrolling

Conditions

Chronic Rhinosinusitis (CRS) With and Without Nasal Polyps
Chronic Rhinosinusitis (CRS)

Study type

Observational

Funder types

Other

Identifiers

NCT06815211
GenreCRS_2024_V1.0

Details and patient eligibility

About

The objective of the study is to establish a registry of patients diagnosed with Chronic Rhinosinusitis with and without Nasal Polyps (CRSwNP/CRSsNP) to collect comprehensive longitudinal real-world evidence from specialised treatment centres in Germany. The primary analysis will concentrate on the treatment efficacy and safety of biologic drugs with a focus on defining disease Control, Remission, and Cure as well as to validate the corresponding clinical evaluation criteria.

Full description

The German national CRS registry (Genre CRS) is a nationwide registry for patients with CRSsNP and CRSwNP that aims to include more than 250 centres in Germany. Genre CRS is operated by the German Societies of Allergology (AeDA) and Otorhinolaryngology (DGHNO) and is based on most advanced digital health technologies, including a wide variety of collected parameters. Additionally, patient-reported outcome measures will be captured via a smart phone app and submitted directly to the registry database. This registry is the first of its kind in Germany. It will be the foundation for answering many critical/pivotal research questions that depend on high quality, extensive longitudinal data provided by the registry for future studies.

One important field of application will be the long-term assessment of RWE on therapeutic antibodies, also known as "biologics". Biologics are a novel treatment option for patients with severe CRSwNP and have led to tremendous treatment success. Chronically ill patients with a long history of severe symptoms and impaired quality of life can now experience a significant improvement in CRSwNP symptoms when treated with a biologic, which has prompted the discussion about disease Control, Remission, and even Cure. So far, internationally accepted and clinically evaluated definitions of these terms are lacking, but would greatly assist clinicians in developing therapeutic strategies, particularly for the long-term management of chronically affected patients. The criteria currently in use, although generally accepted, are not evidence-based and do not reflect the perspectives of patients and healthcare providers. An international expert working group of the European Academy for Allergy and Clinical Immunology (EAACI) has therefore developed such criteria, which now need to be clinically evaluated and validated using the comprehensive longitudinal data from Genre CRS.

Data collection includes a variety of parameters involved in the treatment with biologics, analysis of their long-term efficacy and safety including but not limited to:

  • Polyp Size
  • SNOT22
  • Visual analog scales for nasal congestion, rhinorrhea, pressure/facial pain, sense of smell
  • Olfactory function
  • Necessity for rescue treatment (sinus surgery, OCS)
  • Parameters of co-morbid diseases
  • Type 2 biomarkers

Enrollment

500 estimated patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients above the age of 12 years
  • Patients who are diagnosed with CRS according to internationally valid guidelines (EPOS 2020)
  • Patients who provide written informed consent or by a legal representative

Exclusion criteria

  • Patients below the age of 12 years at initiation
  • Patients who do not provide written consent or withdraw their consent

Trial design

500 participants in 3 patient groups

sinus surgery
Description:
all patients who received sinus surgery during the observation period
biologic treatment
Description:
all patients who are treated with a biologic drug
non-biologic, non-surgery
Description:
all patients without surgery or biologic treatment during observation period

Trial contacts and locations

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Central trial contact

Jan Hagemann, Dr. med.; Friederike Bärhold, Dr. med.

Data sourced from clinicaltrials.gov

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