Chronic Rhinosinusitis Trial, Recruiting
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 18 years old or older
- You have been officially diagnosed with chronic rhinosinusitis (a long-term sinus condition) according to recognized medical guidelines
- A CT scan taken within the last 6 months shows sinus disease affecting both sides of a specific sinus area (the ethmoid sinuses, located between your eyes), and this scan was taken at least 6 months after any previous sinus surgery if you have had one
- The same CT scan also shows disease affecting both of your frontal sinuses (located in your forehead) or the passages leading to them
- Your sinus symptom score on a standard questionnaire (called SNOT-22) is 30 or higher, meaning your symptoms are significantly affecting your quality of life
- Previous treatments such as medications have not worked well enough, and your doctor considers you a suitable candidate for sinus surgery on both sides
- You are willing and able to sign a consent form agreeing to take part
- You are willing and able to attend all required follow-up appointments and assessments during the study
Who may not be able to join:
- You have a tumor (cancerous or non-cancerous) inside your nasal cavity
- You have a specific type of nasal polyp called antrochoanal polyps
- You have previously had a full removal of a structure inside your nose called the middle turbinate
- There are signs or suspicion of a serious fungal sinus infection, such as bone damage on your CT scan or dead tissue in the sinuses
- You have a history of a gap in the thin bone near your sinuses or a leak of the fluid that surrounds your brain and spinal cord
- You are currently receiving chemotherapy or immunotherapy for another condition
- Your symptoms are currently too severe to safely have surgery (for example, a very high fever over 102.5°F, or serious complications such as an eye or brain infection, blood clot, or confusion)
- You have previously had complications from sinus surgery or balloon sinus procedures, such as a spinal fluid leak or injury to the skull base or eye area
- You have a condition called primary ciliary dyskinesia, which affects tiny hair-like structures in the airways
- You have a condition that requires you to regularly take steroid tablets to manage it, such as a certain type of lung disease (confirm with trial site)
- There is significant damage, ulceration, or erosion of the tissue inside your nose found during a nasal examination
- You have had an active nasal or upper respiratory infection, including COVID-19, within the 2 weeks before your first study appointment
- You are allergic or have had a reaction to a drug called paclitaxel or similar medicines
- You have taken biologic medications (a type of specialist drug) in the 6 months before screening, or you expect to take them in the next 24 months
- You have taken steroid tablets by mouth in the 30 days before your first study appointment
- You are planning to have a procedure to reduce nerves at the back of the nose in the next 24 months
- You have previously been unable to tolerate a camera examination inside your nose (nasal endoscopy)
- You have another medical condition that could affect how the study team assesses you or that could put your safety at risk, such as severe lung or breathing problems
- You are pregnant or planning to become pregnant during the first 12 months of being in the study
- You have had any nasal or sinus surgery of any kind in the 6 months before your first study appointment
- You have previously had a specific advanced type of frontal sinus surgery called a Draf III procedure, or this type of surgery is expected to be part of your treatment in this study
- Your surgery during the study did not include treatment of both ethmoid and both frontal sinuses as required
- Your planned surgery is expected to include steroid-releasing implants or non-dissolving packing or stents placed in the nose
- Your surgery during the study was stopped or not completed for any reason
- Your life expectancy is less than 2 years
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.
Contact this trial
Principal Investigator: Noem Cohen, MD, University of Pennsylvania
Phone: 6123250226
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
Where this trial is recruiting
Primary endpoints
Primary safety; Primary efficacy endpoint
Can't join this trial?
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.