SOLFAMU Study of Nasal Brushing Collected OLFActory MUcosa Samples in the Diagnosis of Human Encephalopathies
Primary Purpose
Encephalopathy, HIV-encephalopathy, Alzheimer Dementia
Status
Recruiting
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Nasal Brushing
Sponsored by
About this trial
This is an interventional diagnostic trial for Encephalopathy
Eligibility Criteria
Inclusion criteria for cases:
- age>18 years;
- signing a written informed consent (by the patients or his/her legal representant);
- clinical suspect of encephalopathy (acute or subacute) including acute encephalitis, neurodegenerative disorders and HIV-associated neurocognitive disorders.
Inclusion criteria for controls:
- age>18 years;
- signing a written informed consent (by the patients or his/her legal representant); • clinical indication for rhinoscopy for stenotic disease of nasal sept or turbinates.
Exclusion criteria:
- Nasal anatomical abnormalities precluding the execution of nasal brushing;
- Serious general conditions and/or comorbidities in patients for whom nasal brushing may be a risk factor precipitating their pre-existing condition;
- Anti-coagulant treatment.
Sites / Locations
- University of TorinoRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Brushing
Arm Description
Patients will undergo nasal brushing as further described additionally to other gold standard practices according to the suspected aetiology (brain MRI, lumbar puncture, plasma tests, etc.)
Outcomes
Primary Outcome Measures
Diagnostic concordance with gold standard diagnostic procedures
Positive and negative predictive values and correct classification rates of OM tests versus gold standard diagnostic procedures
Secondary Outcome Measures
Side effects of the nasal brushing
Prevalence of side effects reported during the brushing and up to 6 months afterwards
Cytological and immunohistochemistry examination of nasal brushing smear (neuronal abnormalities and expression of specific markers according to the different aetiologies)
Prevalence of samples showing: abnormalities in cytological examination, antiOMP (Olfactory Marker Protein) positive cells, white blood cells and subtypes.
OM markers of neuronal damage and amyloid deposition
Quantification of tau, p-tau, 1-42 beta amyloid, S100beta, alpha synuclein, TDP-43 (TAR DNA-binding protein 43) on cell blocks and supernatant
Full Information
NCT ID
NCT02951559
First Posted
October 27, 2016
Last Updated
May 19, 2022
Sponsor
University of Turin, Italy
1. Study Identification
Unique Protocol Identification Number
NCT02951559
Brief Title
SOLFAMU Study of Nasal Brushing Collected OLFActory MUcosa Samples in the Diagnosis of Human Encephalopathies
Official Title
Study of Nasal Brushing Collected OLFActory MUcosa Samples in the Diagnosis of Human Encephalopathies
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 2016 (undefined)
Primary Completion Date
February 2023 (Anticipated)
Study Completion Date
February 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Turin, Italy
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Encephalopathies are a group of central nervous system (CNS) affection with heterogeneous etiology. Several causes have been recognized including neurodegenerative, vascular, infectious, autoimmune, toxic or allergic affections or secondary to systemic disorders. While 30-50% of acute encephalitis remains without etiological definition, definitive criteria for neurodegenerative diseases are usually unavailable in vivo and possible or probable definitions are used. The Olfactory mucosa (OM) is the part of the nasal mucosa that carries the specialized sensory organ for the modality of smell; the olfactory epithelium is composed of five principal cell types including olfactory receptor neurons. A sample of OM may be collected through a rhinoscopy-guided brushing: it is well-accepted by patients, not-contraindicated in patients with raised intracranial pressure and associated with almost no side-effects. Nasal brushing has recently been proposed for the in vivo diagnosis of Creutzfeldt-Jakob disease (CJD).
Aims of the project are:
Training of ear throat and nose (ETN), Infectious disease (ID) and neurology (NEU) specialists in the technique of nasal brushing;
Conducting a prospective study comparing the use of nasal brushing with gold-standard criteria in the diagnosis of Encephalopathies;
Increasing the diagnostic and prognostic power in the diagnosis of encephalopathies.
A prospective, case control, multicentric study enrolling 400 patients and 100 controls (patients with nasal stenosis undergoing rhinoscopy for clinical reasons). Patients will be diagnosed and followed according to international guidelines and local clinical practice. Cerebrospinal fluid and magnetic resonance imaging will be used, where indicated, for the diagnosis according to the clinical or radiological suspect.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Encephalopathy, HIV-encephalopathy, Alzheimer Dementia
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Model Description
Diagnostic study
Masking
None (Open Label)
Allocation
N/A
Enrollment
250 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Brushing
Arm Type
Experimental
Arm Description
Patients will undergo nasal brushing as further described additionally to other gold standard practices according to the suspected aetiology (brain MRI, lumbar puncture, plasma tests, etc.)
Intervention Type
Device
Intervention Name(s)
Nasal Brushing
Intervention Description
Nasal brushing will be performed in non-sedated patients as follows. After administration of a local vasoconstrictor (1% epinephrine) with the use of a nasal tampon, inserted into the nasal cavity of the patient to locate the olfactory mucosa lining the nasal vault. A sterile, disposable brush ("Copanflock", "Copan", Brescia, Italy) will be inserted gently rolled on the mucosal surface, withdrawn,and immersed in 0.9% saline solution, UTM (Universal Transporter Medium) or 4% formaldehyde. Two swabs will be collected for each nostril.
Primary Outcome Measure Information:
Title
Diagnostic concordance with gold standard diagnostic procedures
Description
Positive and negative predictive values and correct classification rates of OM tests versus gold standard diagnostic procedures
Time Frame
Single-visit
Secondary Outcome Measure Information:
Title
Side effects of the nasal brushing
Description
Prevalence of side effects reported during the brushing and up to 6 months afterwards
Time Frame
Up to 6 months after the procedure
Title
Cytological and immunohistochemistry examination of nasal brushing smear (neuronal abnormalities and expression of specific markers according to the different aetiologies)
Description
Prevalence of samples showing: abnormalities in cytological examination, antiOMP (Olfactory Marker Protein) positive cells, white blood cells and subtypes.
Time Frame
single-visit
Title
OM markers of neuronal damage and amyloid deposition
Description
Quantification of tau, p-tau, 1-42 beta amyloid, S100beta, alpha synuclein, TDP-43 (TAR DNA-binding protein 43) on cell blocks and supernatant
Time Frame
single-visit
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria for cases:
age>18 years;
signing a written informed consent (by the patients or his/her legal representant);
clinical suspect of encephalopathy (acute or subacute) including acute encephalitis, neurodegenerative disorders and HIV-associated neurocognitive disorders.
Inclusion criteria for controls:
age>18 years;
signing a written informed consent (by the patients or his/her legal representant); • clinical indication for rhinoscopy for stenotic disease of nasal sept or turbinates.
Exclusion criteria:
Nasal anatomical abnormalities precluding the execution of nasal brushing;
Serious general conditions and/or comorbidities in patients for whom nasal brushing may be a risk factor precipitating their pre-existing condition;
Anti-coagulant treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
ANDREA CALCAGNO, MD, DTM&H
Phone
+390114393884
Email
andrea.calcagno@unito.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GIOVANNI DI PERRI, MD, PhD
Organizational Affiliation
University of Torino
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Torino
City
Torino
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea Calcagno, MD
Phone
+390114393884
Email
andrea.calcagno@unito.it
First Name & Middle Initial & Last Name & Degree
Stefano Bonora, MD
First Name & Middle Initial & Last Name & Degree
Giovanni Di Perri, MD, PhD
First Name & Middle Initial & Last Name & Degree
Andrea Calcagno, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
SOLFAMU Study of Nasal Brushing Collected OLFActory MUcosa Samples in the Diagnosis of Human Encephalopathies
We'll reach out to this number within 24 hrs