Nasal Polyps Clinical Trial
— OSTROOfficial title:
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Phase 3 Efficacy and Safety Study Of Benralizumab in Patients With Severe Nasal Polyposis (OSTRO)
Verified date | August 2018 |
Source | Johns Hopkins University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized placebo controlled trial to evaluate the effect of benralizumab on people with severe nasal polyps.
Status | Recruiting |
Enrollment | 400 |
Est. completion date | July 1, 2020 |
Est. primary completion date | July 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Age 18-75 - Severe bilateral nasal polyps (score 5 out of 8) - SNOT-22 score > 30 - At least 70% compliance with inhaled nasal steroid based on daily diary - Minimum weight of 40kg - Negative pregnancy test for documented post menopausal for women Exclusion Criteria: - Any sinus surgery within the past 6 months |
Country | Name | City | State |
---|---|---|---|
United States | Johns Hopkins University School of Medicine | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Total Nasal Polyp Score (NPS) | Bilateral endoscopic polyp score. Maximum score 8 (0-4 per side) with higher score indicating worse outcome. Scores will be compared at visit 3 and visit 11 following 56 weeks of treatment. | 56 weeks | |
Primary | Mean Nasal Blockage Score (NBS) | Change from baseline in the mean nasal blockage score (NBS). Score range is 0-3 with higher score indicating worse outcome. Scores will be compared at visit 3 and visit 11 following 56 weeks of treatment. | 56 weeks | |
Secondary | Sino-Nasal Outcome Test (SNOT)-22 Score | Change from baseline in the SNOT-22 symptom score. Score range is 0-110 with higher score indicating worse symptoms. Scores will be compared at visit 3 and visit 11 following 56 weeks of treatment. | 56 | |
Secondary | Time to Nasal Polyp Surgery | Time to nasal polyp surgery from baseline will be compared during 56 weeks of treatment. | 56 weeks | |
Secondary | CT score | Polyp size will be determined by CT scan using the Lund-Mackay score (range 0-10) with higher score indicating bigger polyp size. Scores will be compared at visit 3 and visit 11 following 56 weeks of treatment. | 56 weeks | |
Secondary | Smell Test | Change from baseline in the University of Pennsylvania Smell Identification Test (UPSIT). Score range is 0-40. Scores will be compared at visit 3 and visit 11 following 56 weeks of treatment. | 56 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT02071667 -
Association of Periostin Levels and Chronic Sinusitis
|
N/A | |
Completed |
NCT01623310 -
12-Month OL Intranasal Fluticasone Propionate BID Using OptiNose Device
|
Phase 3 | |
Completed |
NCT02024659 -
Effects and Safety of Budesonide Inhalation Suspension Via Transnasal Nebulization in Nasal Polyps
|
Phase 2/Phase 3 | |
Completed |
NCT00215787 -
Investigation of the Association Between Nasal Polyposis and Extraesophageal Reflux Disease
|
N/A | |
Completed |
NCT04996576 -
Infrazygomatic Versus Intranasal Injection Sphinopalatine Ganglion Blockade Effect on Surgical Field in FESS
|
N/A | |
Recruiting |
NCT03963648 -
NO Measurements in Screening for Asthma and OSA, in Patients With CRSwNP
|
N/A | |
Recruiting |
NCT05094570 -
Interleukin-4Ra Blockade by Dupilumab Decreases Staphylococcus Colonization and Increases Microbial Diversity in CRSwNP
|
Phase 4 | |
Recruiting |
NCT05009758 -
Moving Towards Precision Medicine in United Airways Disease: Unraveling Inflammatory Patterns in Asthmatic Patients With or Without Nasal Polyps
|
N/A | |
Completed |
NCT00731185 -
Mometasone Furoate Nasal Spray for Treatment of Nasal Polyposis After Surgery (Study P03218)
|
Phase 3 | |
Active, not recruiting |
NCT03943121 -
The Effects of Steroid-eluting Stent Implant for the Treatment of Eosinophilic Chronic Rhinosinusitis With Nasal Polyps
|
N/A | |
Active, not recruiting |
NCT03704415 -
Aggravated Airway Inflammation: Research on Genomics and Optimal Operative Treatment (AirGOs Operative)
|
N/A | |
Not yet recruiting |
NCT06070311 -
Wound Healing After Endoscopic Sinus Surgery
|
N/A | |
Completed |
NCT02879929 -
Development and Validity of the DyNaChron Questionnaire for Chronic Nasal Dysfunction
|
N/A | |
Recruiting |
NCT05672030 -
Role of IL-5R Signaling in Non-eosinophil Upper Airway Cells in CRSwNP
|
||
Suspended |
NCT04261582 -
Genetics and Genomics of Aspirin Exacerbated Respiratory Disease (AERD)
|
||
Recruiting |
NCT05063981 -
Treatment With Mepolizumab on Patients With Severe Refractory Eosinophilic Asthma With or Without CRSwNP.
|
||
Completed |
NCT05180357 -
RANS. Study in Patients With Severe Eosinophilic Asthma and Nasal Polyps.
|
||
Completed |
NCT00788463 -
A Comparison of Beclomethasone Aqueous Spray and Aerosol Delivery Systems in Nasal Polyps
|
Phase 2 | |
Completed |
NCT01198912 -
Influence of Oral Doxycycline on Wound Healing After Endonasal Endoscopic Sinus Surgery for Chronic Rhinosinusitis With and Without Nasal Polyposis: a Double-blind Randomized Placebo-controlled Trial
|
Phase 2 | |
Completed |
NCT03280537 -
A Clinical Trial of Omalizumab in Participants With Chronic Rhinosinusitus With Nasal Polyps
|
Phase 3 |