Using active anterior rhinomanometry to guide when surgery is needed for nasal obstruction.
Official title: Evaluation of the Reliability of Anterior Active Rhinomanometry as an Independent Tool for Surgical Indication in Nasal Obstruction
Run by Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · NCT07379775 · Data updated 2026-11-12
This test will try whether preoperative rhinomanometry can help decide if adults with nasal obstruction should have septoplasty, turbinate reduction, or rhinoplasty.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer Academic / other |
| Locations | 1 site (Draguignan, Var) |
| Status | Recruiting |
| Started | January 27, 2026 |
| Main results expected | January 2028 |
| Study ends | March 2028 |
| Registry record updated | July 7, 2026 |
| Trial ID | NCT07379775 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (≥18 years) with nasal obstruction who are already scheduled for septoplasty, turbinate reduction, or rhinoplasty and who had preoperative rhinomanometry and consent to participate.
✕Probably not a fit
Patients with nasal polyps, chronic edematous or crusting rhinosinusitis, or current/past sinonasal tumors — who are excluded from this protocol — are unlikely to benefit from AAR as tested here.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study collects preoperative active anterior rhinomanometry (AAR) measurements in adults scheduled for surgical correction of nasal obstruction to determine whether AAR can independently indicate the need for surgery. Participants are adults with nasal obstruction who underwent rhinomanometry and are scheduled for septoplasty ± turbinoplasty ± rhinoplasty; patients with nasal polyps, certain chronic rhinosinusitis forms, or sinonasal tumors are excluded. Investigators will compare AAR results with clinical findings and standard patient-reported outcome scores (for example VAS, NOSE, SNOT-22) to judge whether AAR alone reliably identifies surgical candidates. The protocol is conducted at a regional hospital in Draguignan, France.
Why it matters
Potential benefit: If successful, this could give doctors a simple objective test to standardize surgical decisions and reduce unnecessary or ineffective nasal surgeries.
How similar studies have gone: Rhinomanometry is a well-established objective measure used alongside symptoms and imaging, but relying on it alone as the sole indication for surgery is not widely validated in prior work.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients aged 18 years or older with nasal obstruction (NO). 2. Patients scheduled for surgery: septoplasty ± turbinoplasty ± rhinoplasty for nasal obstruction. 3. Patients who have undergone a preoperative rhinomanometry assessment. 4. Patients consented to participation Exclusion Criteria: 1. Nasal polyps. 2. Chronic edematous-purulent rhinosinusitis (e.g., cystic fibrosis). 3. Crusting rhinosinusitis (e.g., sarcoidosis, granulomatosis with polyangiitis \[Wegener's\]). 4. Current or previously treated nasal or sinus tumors, or patients undergoing tumor work-up
Where it's running
-
Centre Hospitalier de la Dracénie
Draguignan, Var, France Recruiting
Study contacts
- Study coordinator: Sophie Lafond
- Email: sophie.lafond@ch-toulon.fr
- Phone: 0483772062
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.