- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06834477
Impact of Structural and Microenvironmental Abnormalities in Olfactory Cleft on Olfaction in CRS
The Influence of Structural and Microenvironmental Abnormalities in the Olfactory Cleft on Olfactory Function in Patients With Chronic Rhinosinusitis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Olfactory dysfunction (OD) is a critical symptom among patients with CRS, affecting up to 83% of individuals with the condition. Currently, it is considered that the inflammation in olfactory cleft is a central factor contributing to both conductive and sensorineural OD in patients with CRS. Inflammation in the olfactory cleft could impair olfaction by altering the mucosal and mucus microenvironment thereby causing damage to the olfactory neuroepithelium, by physically impeding delivery of odorant-containing air to the olfactory cleft, or a combination of both mechanisms.
Existing studies mainly focus on isolated mechanisms, such as inflammation-induced physical obstruction or injury of olfactory epithelium. However, limited research has explored how structural abnormalities and microenvironmental changes in the olfactory cleft might interact to contribute to olfactory dysfunction. This research aimed to evaluate the relationship between structural abnormalities and microenvironmental changes in the olfactory cleft and their impact on olfactory function in patients with CRS using a multidimensional approach integrating imaging, pathology, and functional analysis.
This is a retrospective study. Patients with CRS admitted for endoscopic sinus surgery (n = 70) and healthy controls undergoing surgery for the deviated septum (n = 10) were included. All the participants had undergone:
Clinical assessment of olfactory function and quality of life
- Olfactory measurements had been conducted preoperatively using the Sniffin' Sticks Test to evaluate olfactory threshold (OT), olfactory discrimination (OD), olfactory identification (OI), and the overall composite scores (TDI). A TDI score > 30.75, 16-30.75, and ≤ 15 indicates normosmia, hyposmia, and anosmia, respectively.
- The 22-item Sino-Nasal Outcome Test (SNOT-22) had been administered to evaluate patient-reported subjective outcomes.
- The Questionnaire of Olfactory Disorders Negative Statements (QOD-NS) was utilized to assess the olfactory-specific quality of life.
- The visual analog scale(VAS)for olfaction was employed to measure patients' self-reported olfaction.
Evaluation of structural abnormalities and patency of the olfactory cleft
Computed tomography scans were obtained in every participant. The anterior boundary of OC is defined by the anterior attachment of the middle turbinate; the posterior boundary corresponding to the anterior face of the sphenoid sinus; the lateral boundaries are defined as the attachment of the middle and/or superior turbinate laterally and the nasal septum medially. The olfactory cleft is further divided into anterior and posterior, divided by the anterior end of the superior turbinate. The olfactory cleft opacification is defined as the normal airway filled with a value representing soft tissue and /or presence of close contact between the nasal turbinates and the nasal septum. The opacification percentage in the anterior olfactory cleft is calculated using the lower margin of the middle turbinate and the cribriform plate as the vertical boundaries. The opacification percentage in the posterior olfactory cleft is calculated using the lower margin of the superior turbinate and the cribriform plate as the vertical boundaries. The olfactory cleft opacifications were graded on a scale of 0-4 by the ratio of the opacified area to the whole area of the corresponding region of the olfactory cleft, with 0 (no opacification), 1 (25%), 2 (25%-50%), 3 (50%-75%), and 4 (>75%). Then we evaluated:
- The original version of olfactory cleft CT score, calculated as the sum of the anterior and posterior olfactory cleft opacification scores, ranged from 1 to 8.
- The modified version of olfactory cleft CT score: CT scores for unilateral olfactory cleft, including the anterior and posterior regions, specifically the left anterior, left posterior, right anterior, and right posterior olfactory cleft, as well as their total sum. Additionally, a more detailed assessment is performed by recording whether opacification is present at the apex and the middle-lower portion of each olfactory cleft subregion. Each subregion is further divided into anterior, middle, and posterior areas, with each area being independently assessed. A score of 1 is assigned if opacification is observed, and 0 if absent.
To further quantify the impact of olfactory cleft obstruction on olfactory airflow, this study employs three-dimensional modeling and computational fluid dynamics (CFD) analysis of the nasal cavity based on CT imaging data of sinuses. The air flow, velocity, pressure, and air flow ratio in the olfactory cleft were obtained by the hydrodynamics analysis method.
Evaluation of the mucus and mucosal microenvironment in the olfactory cleft
- Patients with CRS were categorized into two clinical phenotypes, CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP), based on histology and physical examination.
- To investigate the inflammatory phenotypes of CRS, hematoxylin and eosin (H&E) staining were performed to identify the predominant inflammatory cell types within the lamina propria. Patients with CRS were divided into eosinophilic CRS and non-eosinophilic CRS. The eosinophilic phenotype of CRS was defined when the frequency of tissue eosinophils exceeded 10% of the total infiltrating cells per high-power field.
- Olfactory cleft mucus was collected to quantify the level of olfactory cleft mucus galectin-10 and eosinophil-derived neurotoxin (EDN) using commercial human enzyme-linked immunosorbent assay kits. Th1/Th2-related cytokines, including IL-2, IL-4, IL-5, IL-6, IFN-γ, TNF, and IL-10, were detected using a flow cytometry-based bead array (CBA) capture assay.
- Olfactory cleft mucosal specimens were collected from the anterior portion of the superior turbinate using a through-cut forceps during surgery for immunohistochemical analysis of olfactory marker protein (OMP), to evaluate the expression levels of mature olfactory neurons.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Dawei Wu, MD, PhD
- Phone Number: +86-10-13522503401
- Email: davidwuorl@163.com
Study Locations
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Haidian District
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Beijing, Haidian District, China, 10019
- Department of Otolaryngology Head and Neck Surgery, Peking University Third Hospital, Beijing, People's Republic of China
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Contact:
- Dawei Wu, MD, PhD
- Phone Number: +86-10-13522503401
- Email: davidwuorl@163.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria for patient group:
- Diagnosed with CRS based on the diagnostic criteria of the EPOS guideline.
- Provision of signed and dated informed consent form.
- Patients with CRS admitted to the hospital awaiting endoscopic sinus surgery.
Inclusion Criteria for control group:
- Healthy controls undergoing surgery for the deviated septum.
- Provision of signed and dated informed consent form.
Exclusion Criteria for patient group:
- Those who have taken oral glucocorticoids, antibiotics, anti-leukotrienes, and antihistamines within four weeks.
- Patients who have had prior sinus surgery.
- Patients with fungal sinusitis, inverted papilloma, or other nasal diseases.
- Patients with a diagnosis of immune suppression or suspicion of malignancy that may be affecting the nose/paranasal sinuses.
- Patients who are mentally or physically unable to perform olfactory tests
Exclusion Criteria for control group:
- Patients with nasal polyps, sinusitis, nasal cavity tumors and other diseases.
- Patients with hyposmia or anosmia.
- Patients with diagnosed neurodegenerative disease.
- Patients who are mentally or physically unable to perform olfactory tests.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients with CRS admitted for endoscopic sinus surgery
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low-dose CT is taken
Other Names:
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healthy controls undergoing surgery for the deviated septum
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low-dose CT is taken
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sniffin Sticks Test
Time Frame: Immediately before surgery
|
The test consists of odorous rods that are presented to the patient's nose. It consists of 3 parts different, with 3 sets of corresponding sticks: an olfactory threshold test, an olfactory discrimination test and an olfactory identification test. The final TDI score, out of 48, is the sum of the olfactory threshold, discrimination and identification scores. |
Immediately before surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The 22-item Sino-Nasal Outcome Test (SNOT-22)
Time Frame: Immediately before surgery
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Immediately before surgery
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|
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Visual analog scale(VAS)for olfaction
Time Frame: Immediately before surgery
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numerical rating scale from 0 (no smell) to 10 (perfect smell)
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Immediately before surgery
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The Questionnaire of Olfactory Disorders Negative Statements (QOD-NS)
Time Frame: Immediately before surgery
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The QOD-NS comprises 17 negatively phrased statements, each rated on a scale from 0 (disagree) to 3 (agree), yielding a maximum score of 51.
Higher QOD-NS scores indicate a poorer quality of life.
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Immediately before surgery
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The original version of olfactory cleft CT score
Time Frame: during routine preoperative CT imaging
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during routine preoperative CT imaging
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The modified version of olfactory cleft CT score
Time Frame: during routine preoperative CT imaging
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during routine preoperative CT imaging
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Airflow velocity in the olfactory cleft
Time Frame: Immediately after CT scans
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one of the airflow parameters in the olfactory cleft that can be obtained by CFD analysis
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Immediately after CT scans
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Mass flowrate in the olfactory cleft
Time Frame: Immediately after CT scans
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One of the airflow parameters in the olfactory cleft that can be obtained by CFD analysis
|
Immediately after CT scans
|
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Airflow ratio in the olfactory cleft
Time Frame: Immediately after CT scans
|
one of the airflow parameters in the olfactory cleft that can be obtained by CFD analysis.
The airflow ratio was calculated as the mass flowrate through the OC relative to the total airflow rate through the nasal cavity.
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Immediately after CT scans
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The level of eosinophil-derived neurotoxin, galectin-10 and otherTh1/Th2-related cytokines in olfactory cleft mucus
Time Frame: Immediately after surgery
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The levels of galectin-10 and eosinophil-derived neurotoxin (EDN) in olfactory cleft mucus were measured by commercial human enzyme-linked immunosorbent assay kits.
Th1/Th2-related cytokines, including IL-2, IL-4, IL-5, IL-6, IFN-γ, TNF, and IL-10, were detected using a flow cytometry-based bead array (CBA) capture assay.
|
Immediately after surgery
|
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Clinical phenotypes classification:CRS with nasal polyps (CRSwNP) or CRS without nasal polyps (CRSsNP)
Time Frame: During preoperative physical and imaging examinations
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During preoperative physical and imaging examinations
|
|
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Histopathological phenotypes classification: eosinophilic CRS or non-eosinophilic CRS
Time Frame: Immediately after surgery
|
Hematoxylin and eosin (H&E) staining are performed to identify the predominant inflammatory cell types within the lamina propria.
Patients with CRS were divided into eosinophilic CRS and non-eosinophilic CRS.
|
Immediately after surgery
|
|
Immunohistochemical staining of olfactory marker protein (OMP) in olfactory epithelium
Time Frame: Immediately after surgery
|
The OMP is a kind of biomarker for mature olfactory sensory neurons.
This parameter may indicate the inflammation-induced neurological damage in olfactory epithelium.
|
Immediately after surgery
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9059102
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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