search
Back to results

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
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Montelukast focused on measuring Montelukast, Chronic Rhinosinusitis with Nasal Polyps

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
October 8, 2021
Last Updated
March 6, 2022
Sponsor
Assiut University
search

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
Fokkens WJ, Lund VJ, Mullol J, Bachert C, Alobid I, Baroody F, Cohen N, Cervin A, Douglas R, Gevaert P, Georgalas C, Goossens H, Harvey R, Hellings P, Hopkins C, Jones N, Joos G, Kalogjera L, Kern B, Kowalski M, Price D, Riechelmann H, Schlosser R, Senior B, Thomas M, Toskala E, Voegels R, Wang de Y, Wormald PJ. EPOS 2012: European position paper on rhinosinusitis and nasal polyps 2012. A summary for otorhinolaryngologists. Rhinology. 2012 Mar;50(1):1-12. doi: 10.4193/Rhino12.000.
Results Reference
background
PubMed Identifier
27042129
Citation
Langdon C, Mullol J. Nasal polyps in patients with asthma: prevalence, impact, and management challenges. J Asthma Allergy. 2016 Mar 14;9:45-53. doi: 10.2147/JAA.S86251. eCollection 2016.
Results Reference
background
PubMed Identifier
12903683
Citation
Johansson L, Akerlund A, Holmberg K, Melen I, Bende M. Prevalence of nasal polyps in adults: the Skovde population-based study. Ann Otol Rhinol Laryngol. 2003 Jul;112(7):625-9. doi: 10.1177/000348940311200709.
Results Reference
background
PubMed Identifier
27544740
Citation
Wang X, Zhang N, Bo M, Holtappels G, Zheng M, Lou H, Wang H, Zhang L, Bachert C. Diversity of TH cytokine profiles in patients with chronic rhinosinusitis: A multicenter study in Europe, Asia, and Oceania. J Allergy Clin Immunol. 2016 Nov;138(5):1344-1353. doi: 10.1016/j.jaci.2016.05.041. Epub 2016 Jul 15.
Results Reference
background
PubMed Identifier
18167126
Citation
Scadding GK, Durham SR, Mirakian R, Jones NS, Drake-Lee AB, Ryan D, Dixon TA, Huber PA, Nasser SM; British Society for Allergy and Clinical Immunology. BSACI guidelines for the management of rhinosinusitis and nasal polyposis. Clin Exp Allergy. 2008 Feb;38(2):260-75. doi: 10.1111/j.1365-2222.2007.02889.x. Epub 2007 Dec 20.
Results Reference
background
PubMed Identifier
18722209
Citation
Joe SA, Thambi R, Huang J. A systematic review of the use of intranasal steroids in the treatment of chronic rhinosinusitis. Otolaryngol Head Neck Surg. 2008 Sep;139(3):340-7. doi: 10.1016/j.otohns.2008.05.628.
Results Reference
background
PubMed Identifier
22410935
Citation
Rudmik L, Schlosser RJ, Smith TL, Soler ZM. Impact of topical nasal steroid therapy on symptoms of nasal polyposis: a meta-analysis. Laryngoscope. 2012 Jul;122(7):1431-7. doi: 10.1002/lary.23259. Epub 2012 Mar 12.
Results Reference
background
PubMed Identifier
30810118
Citation
Fokkens W, Desrosiers M, Harvey R, Hopkins C, Mullol J, Philpott C, Alobid I, Anselmo-Lima WT, Bachert C, Baroody F, Bernal-Sprekelsen M, von Buchwald C, Cervin A, Cohen N, Constantinidis J, De Gabory L, Douglas R, Gevaert P, Hafner A, Hellings P, Joos G, Kalogjera L, Kern R, Knill A, Kocks J, Landis BN, Limpens J, Lebeer S, Lourenco O, Matricardi PM, Meco C, O Mahony L, Reitsma S, Ryan D, Schlosser R, Senior B, Smith T, Teeling T, Tomazic PV, Toppila-Salmi S, Wang DY, Wang D, Zhang L, Lund V. EPOS2020: development strategy and goals for the latest European Position Paper on Rhinosinusitis. Rhinology. 2019 Jun 1;57(3):162-168. doi: 10.4193/Rhin19.080.
Results Reference
background
PubMed Identifier
12532084
Citation
Holgate ST, Peters-Golden M, Panettieri RA, Henderson WR Jr. Roles of cysteinyl leukotrienes in airway inflammation, smooth muscle function, and remodeling. J Allergy Clin Immunol. 2003 Jan;111(1 Suppl):S18-34; discussion S34-6. doi: 10.1067/mai.2003.25.
Results Reference
background
PubMed Identifier
22830292
Citation
Cao Y, Wang J, Bunjhoo H, Xie M, Xu Y, Fang H. Comparison of leukotriene receptor antagonists in addition to inhaled corticosteroid and inhaled corticosteroid alone in the treatment of adolescents and adults with bronchial asthma: a meta-analysis. Asian Pac J Allergy Immunol. 2012 Jun;30(2):130-8.
Results Reference
background

Learn more about this trial

Role of Montelukast in the Management of Chronic Rhinosinusitis With Nasal Polyps.

We'll reach out to this number within 24 hrs