Chronic Rhinosinusitis Trial, Not Yet Recruiting NCT07046117 Sponsor: Medical University of Vienna Condition: Chronic Rhinosinusitis
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Chronic Rhinosinusitis Trial, Not Yet Recruiting

NCT07046117
Not Yet Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 18 and 99 years old and willing to take part in the study
  • You have been formally diagnosed with asthma by a doctor
  • You are receiving treatment for severe asthma at the highest recommended treatment levels (known as GINA/DAL step 4 or 5)
  • Your asthma is not well controlled despite taking high-dose inhaled medicines, shown by one or more of the following: a low asthma control score (ACT below 20 or ACQ above 0.75), needing steroid tablets at least twice in the past 12 months, being hospitalised for asthma in the past 12 months, or having reduced lung function (below 80% of what is expected for you)
  • You have a specific marker of airway inflammation (called FeNO) of 20 or above, measured by a breathing test
  • You have a raised level of certain immune cells (eosinophils) in your blood or airway samples, above set thresholds (confirm with trial site for exact values)
  • You have a mucus score of 1 or higher, as assessed by the study team
  • You have given your written agreement (informed consent) to take part before any study procedures begin
  • If you have previously taken a biologic medicine (a type of specialist injection treatment) for asthma or nasal polyps, enough time must have passed since your last dose — at least 3 months or 3 times the medicine's half-life, whichever is longer (confirm with trial site)
  • For one specific group in the trial: you have nasal polyps confirmed by a scan or camera examination of your nose

Who may not be able to join:

  • You are currently taking a biologic medicine, or have taken one within the past 12 weeks, or have ever been treated with tezepelumab specifically
  • You are pregnant (this will be checked with a urine test)
  • You have a physical condition inside your nose or airways that would make it impossible to carry out the procedures required in the study (confirm with trial site)
  • You have another serious lung condition such as bronchiectasis, pulmonary fibrosis, emphysema, cystic fibrosis, primary ciliary dyskinesia, or lung cancer
  • You have any known parasitic infection
  • Your nasal polyps are caused by something other than a specific type of airway inflammation called Type 2 inflammation (confirm with trial site)
  • You have certain other conditions that can cause asthma-like symptoms and raised eosinophil levels, such as EGPA, allergic bronchopulmonary aspergillosis, or hypereosinophilic syndrome (confirm with trial site)
  • There are medical reasons why it would not be safe for you to have a small tissue sample (biopsy) taken from your airways
  • You have a mental health condition that makes it difficult to fully understand what taking part in the study involves
  • You have other significant health conditions that the study team considers would affect your participation (confirm with trial site)
  • You are taking immunosuppressant medicines such as cyclosporine
  • You currently misuse drugs or alcohol
  • You are a current smoker, or you stopped smoking less than 6 months ago

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Marco Idzko, MD, PhD, Medical University of Vienna

Phone: +43140400

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Not Yet Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 October 2025
Est. completion
31 January 2028

Where this trial is recruiting

🇦🇹 Austria

Primary endpoints

Change in cell index

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov