Role of Montelukast in the Management of Chronic Rhinosinusitis With Nasal Polyps.
Primary Purpose
Montelukast, Chronic Rhinosinusitis With Nasal Polyps
Status
Active
Phase
Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
Montelukast
Prednisolone
Fluticasone Furoate
Sponsored by
About this trial
This is an interventional treatment trial for Montelukast focused on measuring Montelukast, Chronic Rhinosinusitis with Nasal Polyps
Eligibility Criteria
Inclusion Criteria:
- - 1- Adult patients (aged 18 years and over)
- 2- Bilateral denovo nasal polyps confirmed by nasal endoscopy and CT scan.
Exclusion Criteria:
- - 1- CRS patients without nasal polyposis.
- 2- Patient with unilateral nasal polyp.
- 3- Revision cases (history of previous surgical treatment).
- 4- Patient with fungal rhinosinusitis..
- 5- Pregnancy and lactation.
- 6- Malignancies.
Sites / Locations
- Assiut University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Montelukast Group
Control Group
Arm Description
Patients in group A (interventional group) will be treated with fluticasone furoate nasal: (50 micrograms /spray ) 100 micrograms (2 sprays) in each nostril twice daily plus oral montelukast (montelukast 10 mg, once a day) for 3 monthes and oral Prednisolone 40 mg/day for two weeks.
Subjects in treatment group B will receive topical and systemic steroids in an identical regimen only.
Outcomes
Primary Outcome Measures
Change at nasal polyp size
Each CRSwNP patient will undergo nasal endoscopy to score the polyp size (0-4) in both nasal cavities using a modified Lildholdt scoring system:
0 = no nasal polyps.
small nasal polyps not reaching the inferior border of the middle turbinate.
nasal polyps reaching beyond the inferior border of the middle turbinate.
large nasal polyps reaching the lower edge of the inferior turbinate
very large nasal polyps in contact with the floor of the nasal cavity.
Secondary Outcome Measures
Nasal symptoms.
All participants will asked to score five sinonasal symptoms (nasal congestion/obstruction, anterior rhinorrhea, posterior rhinorrhea, loss of smell, and facial pain) from 0 to 4.
0 = symptom-free/no symptom.
mild symptom.
moderate symptom.
severe symptom.
very severe symptom. This score will be assessed at the screening visit and follow-up visits at 4, 8 and 12 weeks. The total five-symptom score (T5SS) obtained with the sum of the individual symptoms (0-20).
Radiological evaluation
CT scan of the nose and paranasal sinuses will performed to all patients before and after the treatment and staged using the Lund-Mackay (LMK) scoring system where each sinus (maxillar, anterior ethmoidal, posterior eth-moidal, frontal, esphenoidal) is scored for opacification (0, no opacity; 1, partial opacity; 2, total opacity), and the ostiomeatal complex is scored 0 (no obstruction) or 2 (obstruction). The uni-lateral score goes from 0 to 12 whereas the bilateral score goes from 0 to 24.
Quality of life score
Subjects will complete validated questionnaire related to general quality of life lCSD (International Classification of Sinus Disease) before and after treatment. The ICSD records patients' symptoms of facial pain and pressure; headache ;nasal blockage Or congestion; nasal discharge; disturbance of smell; and Over all discomfort on a 0 to 10 ordinal scale.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05143502
Brief Title
Role of Montelukast in the Management of Chronic Rhinosinusitis With Nasal Polyps.
Official Title
Role of Montelukast in the Management of Chronic Rhinosinusitis With Nasal Polyps.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
March 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the work is to examine the efficacy of montelukast as an adjunct to steroid therapy in patients with chronic rhinosinusitis with nasal polyps.
Detailed Description
Population and Methods The study will be conducted at the otorhinolaryngology department in Assiut University Hospital.
Study design: prospective randomized controlled trial.
.
Methodology:
After fulfilling all inclusion and exclusion criteria all patients will be subjected to
A. Full history taking including :
Personal History
History of sinonasal symptoms (nasal obstruction, nasal discharge, headache, hyposmia, sneezing, itching, facial pain…etc)
History of nasal surgery.
Other ENT symptoms
General symptoms suggestive of atopy
History of general medical illness.
B. Examination :
1. General examination.
2. Full ENT examination.
3. Nasal endoscopy.
C. Investigations :
Multi-slice computer tomography (MSCT) of nose and paranasal sinuses axial, coronal and sagittal cuts without contrast .
D. Management :
Patients will be divided into 2 equal groups. Patients in group A will be treated with fluticasone furoate nasal: (50 micrograms /spray ) 100 micrograms (2 sprays) in each nostril twice daily plus oral montelukast (montelukast 10 mg, once a day) for 3 monthes and oral Prednisolone 40 mg/day for two weeks. Subjects in treatment group B will receive topical and systemic steroids in an identical regimen only.
.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Montelukast, Chronic Rhinosinusitis With Nasal Polyps
Keywords
Montelukast, Chronic Rhinosinusitis with Nasal Polyps
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Montelukast Group
Arm Type
Experimental
Arm Description
Patients in group A (interventional group) will be treated with fluticasone furoate nasal: (50 micrograms /spray ) 100 micrograms (2 sprays) in each nostril twice daily plus oral montelukast (montelukast 10 mg, once a day) for 3 monthes and oral Prednisolone 40 mg/day for two weeks.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
Subjects in treatment group B will receive topical and systemic steroids in an identical regimen only.
Intervention Type
Drug
Intervention Name(s)
Montelukast
Intervention Description
Montelukast is a leukotrienes antagonist which has proven efficacious in chronic inflammatory conditions of the airways, including allergic rhinitis, asthma, and aspirin-exacerbated respiratory disease (AERD), all diseases that often coexist with CRSwNP.
We will use oral Montelukast (montelukast 10 mg, once a day) for 3 monthes
Intervention Type
Drug
Intervention Name(s)
Prednisolone
Intervention Description
Oral Prednisolone 40 mg/day for two weeks.
Intervention Type
Drug
Intervention Name(s)
Fluticasone Furoate
Intervention Description
fluticasone furoate nasal: (50 micrograms /spray ) 100 micrograms (2 sprays) in each nostril twice daily
Primary Outcome Measure Information:
Title
Change at nasal polyp size
Description
Each CRSwNP patient will undergo nasal endoscopy to score the polyp size (0-4) in both nasal cavities using a modified Lildholdt scoring system:
0 = no nasal polyps.
small nasal polyps not reaching the inferior border of the middle turbinate.
nasal polyps reaching beyond the inferior border of the middle turbinate.
large nasal polyps reaching the lower edge of the inferior turbinate
very large nasal polyps in contact with the floor of the nasal cavity.
Time Frame
after 12 weeks from the start of treatment
Secondary Outcome Measure Information:
Title
Nasal symptoms.
Description
All participants will asked to score five sinonasal symptoms (nasal congestion/obstruction, anterior rhinorrhea, posterior rhinorrhea, loss of smell, and facial pain) from 0 to 4.
0 = symptom-free/no symptom.
mild symptom.
moderate symptom.
severe symptom.
very severe symptom. This score will be assessed at the screening visit and follow-up visits at 4, 8 and 12 weeks. The total five-symptom score (T5SS) obtained with the sum of the individual symptoms (0-20).
Time Frame
after 12 weeks from the start of treatment
Title
Radiological evaluation
Description
CT scan of the nose and paranasal sinuses will performed to all patients before and after the treatment and staged using the Lund-Mackay (LMK) scoring system where each sinus (maxillar, anterior ethmoidal, posterior eth-moidal, frontal, esphenoidal) is scored for opacification (0, no opacity; 1, partial opacity; 2, total opacity), and the ostiomeatal complex is scored 0 (no obstruction) or 2 (obstruction). The uni-lateral score goes from 0 to 12 whereas the bilateral score goes from 0 to 24.
Time Frame
after 12 weeks from the start of treatment
Title
Quality of life score
Description
Subjects will complete validated questionnaire related to general quality of life lCSD (International Classification of Sinus Disease) before and after treatment. The ICSD records patients' symptoms of facial pain and pressure; headache ;nasal blockage Or congestion; nasal discharge; disturbance of smell; and Over all discomfort on a 0 to 10 ordinal scale.
Time Frame
after 12 weeks from the start of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
- 1- Adult patients (aged 18 years and over)
2- Bilateral denovo nasal polyps confirmed by nasal endoscopy and CT scan.
Exclusion Criteria:
- 1- CRS patients without nasal polyposis.
2- Patient with unilateral nasal polyp.
3- Revision cases (history of previous surgical treatment).
4- Patient with fungal rhinosinusitis..
5- Pregnancy and lactation.
6- Malignancies.
Facility Information:
Facility Name
Assiut University Hospital
City
Assiut
Country
Egypt
12. IPD Sharing Statement
Citations:
PubMed Identifier
22469599
Citation
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Results Reference
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Citation
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Role of Montelukast in the Management of Chronic Rhinosinusitis With Nasal Polyps.
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