Diagnostics of Mycotic Sinusitis in ENT Patients

July 24, 2023 updated by: University Hospital Ostrava

Diagnostics of Mycotic Sinusitis in Patients With Unilateral Obfuscation of the Paranasal Sinus and Patients With Uni-lateral Discharge From the Nasal Cavity

Mycotic sinusitis is a rare inflammatory disease of the paranasal sinuses. In recent years, its occurrence is increasing. Due to this situation, mycotic sinusitis is gaining importance, even though most cases of mycotic sinusitis are limited on paranasal sinuses.

Non-invasive forms of mycotic sinusitis are divided into mycetoma and allergic mycotic sinusitis. Mycetoma (fungus ball) usually affects only one paranasal sinus, most often maxillary sinus. The predisposing factors which participate on development of mycotic sinusitis are not exactly known. Some factors are considered as possible predisposing factors, for example deviation of nasal septum, dental treatment of upper jaw teeth or changes of nasal microbiome.

The diagnosis of fungal sinusitis is problematic. With the increasing number of patients, it is essential to improve the diagnostic process. In present, suspicion of mycotic sinusitis is based on the patient's clinical symptoms and the endoscopic findings in the nasal cavity. Only in some cases nonspecific findings can be observed, such as smelly secretions from the nose, feeling of stuffy nose and pain over the affected sinus. Some patients may be completely asymptomatic, and only in some cases fungal masses can be observed in the nasal cavity. Computed tomography (CT) scans are gaining more and more importance. Typical sign of an affected sinus is obfuscation on CT scan but this sign is not specific for mycotic infection. Central hyperdense foci are also present in some patients, but they are also not specific and can imitate a foreign body. Identifying specific signs on CT scan could help with diagnosing mycotic sinusitis.

Study Overview

Status

Recruiting

Conditions

Detailed Description

To identify specific determining signs for the diagnosis of fungal sinusitis, patients will undergo a series of examinations listed below.

  1. Entrance ear, nose, throat (ENT) examination

    • anamnesis (nasal secretion, nasal obstruction, nose injury, dental procedures on the teeth of the upper jaw, immune disorder)
    • rhinological questionnaires (SNOT-22, rhinoVAS, NOSE score, olfactory questionnaire)
    • ENT examination without endoscope: deviation of the nasal septum or hypertrophy of the nasal conchae, pathological secretion from the nose
    • endoscopic examination of the nose: pathological secretion in the nasal cavity or from the orifice of the sinuses, the presence of fungal masses in the nasal cavity, obstruction of the orifice of the sinuses, the edge of the nasal septum
  2. Computed tomography (CT) examination of the paranasal sinuses

    • evaluation of images in the frontal, sagittal and transverse planes
    • criteria of the affected cavity - complete/partial obscuration of the paranasal sinuses, hyperdense core, usuration or thickening of the bone of the paranasal sinuses
    • anatomical conditions of the nose and paranasal sinuses - the presence of septal deviation, dental pathology, Onodi's cellar, Haller's cellar, lateral recess of the sphenoid sinus
  3. Functional endonasal endoscopic surgery (FESS)

    • method of execution performance of functional endonasal endoscopic surgery - only the affected cavity is being operated, complete cleaning of the affected cavity
    • sampling during surgery (4 in total): two samples for histological examination (sample 1 - mycotic material, sample 2 - mucous of the affected paranasal sinus), sample 3 - mycotic material for culture examination of fungi, sample 4 - mycotic material for elemental analysis using electron microscopy .
  4. postoperative sample analysis

    • elemental analysis (sample 4): before analysis - control X-ray examination of the sample, the presence of hyperdense material on the X-ray image, performing electron microscopy, according to the structure of element evaluation.
    • histological examination (sample 1 and 2): evaluation of the sample 2 - mucosa of the paranasal sinuses - the presence of fungal invasion into the mucosa, inflammatory cellulization in the mucosa, evaluation of the sample 1 (mycotic material) - the presence of hyphae, inflammatory cellulization, calcification.
    • culture examination (sample 3): evaluation of the cultured finding by a microbiologist

Study Type

Interventional

Enrollment (Estimated)

65

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Czech Republic
      • Ostrava, Czech Republic, Czechia, 70852
        • Recruiting
        • University Hospital Ostrava, Department of Otorhinolaryngology and Head and Neck Surgery
        • Contact:
        • Principal Investigator:
          • Simona Polášková, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • age ≥ 18 years
  • patients with unilateral obfuscation of the paranasal sinus and patients with unilateral discharge from the nasal cavity

Exclusion Criteria:

  • serious illness (decompensation phase) - cardiac, liver, kidney disease, can-cer
  • serious psychiatric illnesses
  • pregnancy
  • high operative risk according to The American Society of Anesthesiologists (ASA) ≥ IV
  • disagreement with participation in the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Patient with clinical suspicion of mycotic sinusitis
Patient with clinical suspicion of mycotic sinusitis will undergo an examination as listed in Detailed Description.
Samplings from patient's affected paranasal sinus during endoscopic surgery.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Computer tomography (CT) examination of the paranasal sinuses - images
Time Frame: 3 years
Evaluation of images in the frontal, sagittal and transverse planes - condition assessment.
3 years
Computer tomography (CT) examination of the paranasal sinuses - anatomical conditions of the nose and paranasal sinuses
Time Frame: 3 years
Evaluation of anatomical conditions of the nose and paranasal sinuses - the presence of septal deviation, dental pathology, Onodi's cellar, Haller's cellar, lateral recess of the sphenoid sinus.
3 years
Entrance ENT examination - anamnesis
Time Frame: 3 years
Taking anamnesis from patients to summarize any nasal secretion, nasal obstruction, nose injury, dental procedures on the teeth of the upper jaw or immune disorder.
3 years
Entrance ENT examination - SNOT-22
Time Frame: 3 years
Sino-Nasal Outcome Test-22 (SNOT-22) Questionnaire - The patients will complete a list of symptoms and social/emotional consequences of their nasal disorder. The SNOT-22 is a validated scale that measures sinonasal symptoms in patients with sinusitis. The 22 questions are scored on a scale of 0-5 with a maximum total score of 110. Higher scores represent more symptomatic patients.
3 years
Entrance ENT examination - rhinoVAS
Time Frame: 3 years
Rhino Visual Analogue Scale (RhinoVAS) questionnaire will be used to assess postoperative changes in nasal function ranging from 0 (complete nose patency) to 10 cm (complete nose obstruction).
3 years
Entrance ENT examination - NOSE score
Time Frame: 3 years
A simple, five-question, validated Nasal Obstruction Symptom Evaluation (NOSE) instrument that uses a 20-point scale to capture breathing symptoms, with higher scores indicating more severe symptoms than lower scores. A score of 0 means no problems with nasal obstruction and a score of 100 means the worst possible problems with nasal obstruction.
3 years
Entrance ENT examination - olfactory questionnaire
Time Frame: 3 years
Olfactory questionnaire includes a short examination (test of identification and discrimination with perfumed markers) will be performed.
3 years
Entrance ENT examination - endoscopic examination
Time Frame: 3 years
Endoscopic examination of the nose in order to find any pathological secretion in the nasal cavity or from the orifice of the sinuses, the presence of fungal masses in the nasal cavity, obstruction of the orifice of the sinuses, the edge of the nasal septum.
3 years
Functional endonasal endoscopic surgery (FESS) - sample 1
Time Frame: 3 years
Mycotic material (as sample 1) for histological examination will be taken from patient´s affected cavity during FESS.
3 years
Functional endonasal endoscopic surgery (FESS) - sample 2
Time Frame: 3 years
Mucous of the affected paranasal sinus (as sample 2) for histological examination will be taken from patient´s affected cavity during FESS.
3 years
Functional endonasal endoscopic surgery (FESS) - sample 3
Time Frame: 3 years
Mycotic material for culture examination of fungi (as sample 3) will be taken from patient´s affected cavity during FESS.
3 years
Functional endonasal endoscopic surgery (FESS) - sample 4
Time Frame: 3 years
Mycotic material for elemental analysis using electron microscopy (as sample 4) will be taken from patient´s affected cavity during FESS.
3 years
Postoperative sample analysis - histological examination of sample 1
Time Frame: 3 years
Evaluation of the sample 1 (mycotic material) will be done to find out the presence of hyphae, inflammatory cellulization, calcification.
3 years
Postoperative sample analysis - histological examination of sample 2
Time Frame: 3 years
Evaluation of the sample 2 (mucosa of the paranasal sinuses) will be done to find out the presence of fungal invasion into the mucosa, inflammatory cellulization in the mucosa.
3 years
Postoperative sample analysis - culture examination of sample 3
Time Frame: 3 years
Evaluation of the cultured finding will be done by a microbiologist.
3 years
Postoperative sample analysis - elemental analysis of sample 4
Time Frame: 3 years
Control X-ray examination of the sample will be taken before analysis to find out the presence of hyperdense material on the X-ray image. Performing electron microscopy, according to the structure of ele-ment evaluation.
3 years
Computer tomography (CT) examination of the paranasal sinuses - criteria
Time Frame: 3 years
Evaluation of criteria of the affected cavity - complete/partial obscuration of the paranasal sinuses, hyperdense core, usuration or thickening of the bone of the paranasal sinuses.
3 years
Entrance ENT examination - without endoscope
Time Frame: 3 years
Observation of deviation of the nasal septum or hypertrophy of the nasal concha, patho-logical secretion from the nose.
3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Simona Polášková, MD, University Hospital Ostrava
  • Study Chair: Petr Matoušek, MD, Ph.D., University Hospital Ostrava
  • Study Chair: Michaela Masárová, MD, University Hospital Ostrava
  • Study Chair: Pavel Komínek, Prof., MD, Ph.D., University Hospital Ostrava

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 2, 2023

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

July 13, 2023

First Submitted That Met QC Criteria

July 13, 2023

First Posted (Actual)

July 21, 2023

Study Record Updates

Last Update Posted (Actual)

July 27, 2023

Last Update Submitted That Met QC Criteria

July 24, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • KORLCHHK-2023-Mycosis
  • 06-RVO-FNOs/2023 (Other Grant/Funding Number: University Hospital Ostrava)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is no plan to share individual participant data with other researchers.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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