Sinus stent registry shows symptom relief in chronic sinusitis patients
NCT ID NCT05925985
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study followed 215 people with chronic sinusitis who received a corticosteroid-releasing sinus stent during sinus surgery. Researchers tracked safety and symptom changes over 6 to 12 months using a standard symptom questionnaire. The goal was to confirm the stent's long-term safety and real-world performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- corticosteroid-eluting sinus stent
- What this could lead to
- If results confirm safety and symptom improvement, it supports continued use of these stents to manage chronic sinusitis after surgery.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove the stent caused the improvements. Results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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215 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Sep 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
European CRS population implanted with Propel implants
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient or legally authorized representative (LAR) provides authorization and/or consent per institution and geographical requirements. * Patient has or is intended to receive or be treated with an eligible Medtronic product * Patient is consented within the enrollment window of the therapy received, as applicable Exclusion Criteria: * Patient who is, or is expected to be, inaccessible for follow-up * Participation is excluded by local law * Patient is currently enrolled or plans to enroll in concurrent drug/device study that may confound the PSR results
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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HNO Praxis & Rhinologie Zentrum München
München, Germany
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Helios Dr Horst Schmidt Kliniken
Wiesbaden, Germany
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Imperial College Healthcare NHS Trust - Charing Cross Hospital
London, United Kingdom
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Katholisches Krankenhaus Hagen
Hagen, Germany
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Saint Elisabeth Krankenhaus Köln-Hohenlind
Cologne, Germany
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Städtisches Klinikum Karlsruhe GmbH
Karlsruhe, Germany
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Universitätsklinikum Freiburg Klinik für Hals, Nasen und Ohrenheilkunde
Freiburg im Breisgau, Germany
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Universitätsklinikum Münster Klinik für Hals, Nasen und Ohrenheilkunde
Münster, Germany
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Universitätsklinikum Schleswig-Holstein Campus Lübeck
Lübeck, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Sugar alcohol rinse could soothe sinus pain in cystic fibrosis
- Could a cystic fibrosis drug ease stubborn sinus infections?
- Could viruses and epigenetics be the hidden cause of chronic sinusitis?
- New sinus implant aims to unblock noses and ease facial pain
- Sinus study pulled before it even started
- Scientists hunt for hidden bacteria behind chronic sinusitis