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NCT Number: NCT06815211

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

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.

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Key information

About this study

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

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Primary outcomes

  1. Nasal Polyp Score

    Time frame: 1 year

    Size of nasal polyps from 0-4 per side, with 0=no polyps to 4=large polyps reaching the bottom of the nasal cavity

  2. University of Pennsylvania Smell Identification Test (UPSIT)

    Time frame: 1 year

    smell identification test, 0-40 points, with 0 being the lowest smell function and 40 an excellent smell function

  3. Sniffin' Sticks Identification Test 12

    Time frame: 1 year

    Smell identification test with 12 items, range 0-12, the higher the score, the better the smell function (0=anosmia, 12=normosmia)

  4. Sniffin' Sticks Identification Test 16

    Time frame: 1 year

    Smell identification test with 16 items, range 0-12, the higher the score, the better the smell function (0=anosmia, 12=normosmia)

  5. Sinonasal Outcome Test 22 (SNOT22)

    Time frame: 1 year

    quality of life questionnaire with 22 items (score 0-22). 0=no impairment, 22=maximum impairment in all categories

  6. Rescue Treatment

    Time frame: 1 year

    Number of courses of systemic corticosteroids and number of sinus surgeries necessary due to poor treatmentcontrol or exacerbation of CRS-symptoms

Secondary outcomes

  1. Peak Nasal Inspiratory Flow (PNIF)

    Time frame: 1 year

    measured in l/min

  2. Blood eosinophils

    Time frame: 1 year

    1/µl

  3. Lund-Mackay Score

    Time frame: 1 year

    opacification of nasal sinuses in CT imaging: scores 0-24 with 0=no opacification and 24 complete opacification of all sinuses

  4. Allergic Rhinitis Visual Analogue Scale (AR-VAS)

    Time frame: 1 year

    symptom severity of allergic rhinitis on a visual analogue scale with 0=no symptoms to 10=worst symptoms imaginable

  5. Forced Expiratory Volume in 1 Second (FEV1)

    Time frame: 1 year

    lung function measured in l

  6. Fractional exhaled nitric oxide (FeNO)

    Time frame: 1 year

    measured in ppb

  7. Immunoglobulin E (IgE)

    Time frame: 1 year

    kU/l

Study contacts

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

Friederike Bärhold, Dr. med.

CONTACT

[email protected]

+49611308608273

Jan Hagemann, Dr. med.

CONTACT

[email protected]

+49611308608273

Sponsors and collaborators

Lead sponsor

Ärzteverband Deutscher Allergologen e.V.

Other

Collaborators

  • German Society of Otorhinolaryngology, Head and Neck Surgery

Registry information

Official study title

A Prospective Study for Real-world Evaluation of the Novel European Academy for Allergy and Clinical Immunology (EAACI) Criteria for Disease Control, Remission and Cure in CRSwNP Utilizing the German National CRS Registry (GENRE CRS)

Acronym: GenreCRS

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Feb 7, 2025
Registry last updated
Jun 4, 2025

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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