Preventing Tolerance to Oxymetazoline in Allergic Rhinitis
Primary Purpose
Allergic Rhinitis, Tachyphylaxis, Rhinitis Medicamentosa
Status
Withdrawn
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
oxymetazoline-fluticasone propionate
Oxymetazoline
Sponsored by
About this trial
This is an interventional treatment trial for Allergic Rhinitis focused on measuring allergic rhinitis, rhinitis medicamentosa, imidazolines, corticosteroid
Eligibility Criteria
Inclusion Criteria:
- Male of Female aged 18-65 years.
- Persistent allergic rhinitis with or without asthma.
- Atopy to atleast one allergen on SPT.
- PNIF < 120 L/min (best of 3) and reversibility with OXY >20L/min.
- Ability to give a written informed consent.
- Ability and willingness to comply with the requirements of the protocol.
Exclusion Criteria:
- Recent respiratory tract/sinus infection within the last 2 months. .
- Pregnancy, planned pregnancy or lactation.
- Known or suspected hypersensitivity to any of the IMP's.
- Concomitant use of medicines (prescribed, OTC or herbal) like alpha blockers that may interfere with the trial.
- Nasal Polyposis grade 2+, Deviated nasal septum ≥ 50%
- The use of oral corticosteroids within the last 3 months.
Sites / Locations
- Ninewells Hospital and Medical School (Tayside NHS Trust, University of Dundee)
- Perth Royal Infirmary (Tayside NHS Trust)
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Oxymetazoline-Fluticasone Propionate
Oxymetazoline-placebo
Arm Description
Combination nasal spray with oxymetazoline 0.05% and fluticasone propionate 0.05%
oxymetazoline 0.05% w/v and placebo fluticasone propionate
Outcomes
Primary Outcome Measures
The primary endpoint will be the difference in peak PNIF response to incremental doses of Oxymetazoline [i.e. as a dose response]
Secondary Outcome Measures
Active Anterior Rhinomanometry
Laser Doppler Velocimetry for nasal blood flow
Overnight urinary cortisol creatinine ratio
Nasal nitric oxide levels
Serum eosinophils, ECP
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00846326
Brief Title
Preventing Tolerance to Oxymetazoline in Allergic Rhinitis
Official Title
A Proof of Concept Study to Evaluate if Concomitant Topical Intranasal Steroid Prevents Tolerance and Rebound Congestion Due to Regular Oxymetazoline in Persistent Allergic Rhinitis.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Withdrawn
Why Stopped
The suppliers were unable to provide the investigational medicinal product (IMP)
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Brian J Lipworth
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators wish to evaluate the effects of decongestants like oxymetazoline and the lessening of this effect with time called 'tolerance'. The investigators will demonstrate a reversal of this tolerance with nasal steroids i.e. the investigators will show that nasal steroids protect against tolerance. This will tell us more on how the investigators can make this treatment effective and safe for patients suffering with allergic rhinitis.
Detailed Description
Allergic rhinitis (AR) affects upto 25% of the worldwide population and is associated with asthma, with Scotland having the highest prevalence in the world. Nasal blockage is the main symptom of allergic rhinitis. Nasal blockage affects sleep quality and impairs daytime performance. It is a major cause of sickness absenteeism and has been shown to adversely affect quality of life. The most efficacious class of drugs for nasal blockage in AR are the nasal decongestants (sympathomimetics acting on alpha receptors which unblock the nose). These are available over the counter for routine use by people experiencing nasal blockage. Nasal steroids are the most effective drugs for overall symptoms of allergic rhinitis and are considered first line therapy by recent guidelines. There is widespread belief that prolonged use of decongestant sprays like oxymetazoline can result in a condition of decreased effectiveness called tolerance. It is thought that with time they lose their effectiveness and more and more medication is needed to achieve the same level of decongestion. Also it has been proposed that once stopped, the patient experiences rebound congestion. Long term users of nasal decongestants cannot get off their sprays because of this vicious cycle. These sprays act via stimulating the alpha adrenoreceptors in the nose. It is a poorly understood condition and the mechanism of action is unclear. What is also not clear is the time to onset of tolerance. From studies in the lung we know that tolerance in certain types of adrenoreceptors can be reversed by use of corticosteroids. We have also seen over many years of clinical practice that concomitant use of steroid sprays and decongestants prevents the onset of tolerance and rebound. Anecdotally, patients are often treated with this combination in clinic particularly during a common cold, hayfever season with high pollen counts and acute exacerbations. Therefore, we would like to conduct a proof of concept study to show that a combination nasal spray of decongestant and steroid protects against tolerance. We will also show protection against early rebound congestion. This will enable a new lease of life for allergic rhinitis sufferers, whose quality of life is most affected by nasal blockage and the absence of an effective long term drug strategy for it.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis, Tachyphylaxis, Rhinitis Medicamentosa
Keywords
allergic rhinitis, rhinitis medicamentosa, imidazolines, corticosteroid
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Oxymetazoline-Fluticasone Propionate
Arm Type
Experimental
Arm Description
Combination nasal spray with oxymetazoline 0.05% and fluticasone propionate 0.05%
Arm Title
Oxymetazoline-placebo
Arm Type
Placebo Comparator
Arm Description
oxymetazoline 0.05% w/v and placebo fluticasone propionate
Intervention Type
Drug
Intervention Name(s)
oxymetazoline-fluticasone propionate
Intervention Description
Oxymetazoline 0.05% w/v Fluticasone propionate 0.05% w/w 2 squirts in each nostril twice daily
Intervention Type
Drug
Intervention Name(s)
Oxymetazoline
Intervention Description
oxymetazoline 0.05% w/v and placebo nasal spray 2 squirts in each nostril twice daily
Primary Outcome Measure Information:
Title
The primary endpoint will be the difference in peak PNIF response to incremental doses of Oxymetazoline [i.e. as a dose response]
Time Frame
Pre dose response, after 25, 50, 100, 200 mg/ml of oxymetazoline nasal spray
Secondary Outcome Measure Information:
Title
Active Anterior Rhinomanometry
Time Frame
Pre dose response, after 25, 50, 100, 200 mg/ml of oxymetazoline nasal spray
Title
Laser Doppler Velocimetry for nasal blood flow
Time Frame
Pre dose response, after 50 mg/ml Oxymetazoline and after 200 mg/ml of Oxymetazoline
Title
Overnight urinary cortisol creatinine ratio
Time Frame
post run-in,2 weeks, 4 weeks
Title
Nasal nitric oxide levels
Time Frame
after run-in, 2 weeks, 4 weeks
Title
Serum eosinophils, ECP
Time Frame
post run-in, 2 weeks, 4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male of Female aged 18-65 years.
Persistent allergic rhinitis with or without asthma.
Atopy to atleast one allergen on SPT.
PNIF < 120 L/min (best of 3) and reversibility with OXY >20L/min.
Ability to give a written informed consent.
Ability and willingness to comply with the requirements of the protocol.
Exclusion Criteria:
Recent respiratory tract/sinus infection within the last 2 months. .
Pregnancy, planned pregnancy or lactation.
Known or suspected hypersensitivity to any of the IMP's.
Concomitant use of medicines (prescribed, OTC or herbal) like alpha blockers that may interfere with the trial.
Nasal Polyposis grade 2+, Deviated nasal septum ≥ 50%
The use of oral corticosteroids within the last 3 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian Lipworth, MD, FRCP
Organizational Affiliation
University of Dundee
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ninewells Hospital and Medical School (Tayside NHS Trust, University of Dundee)
City
Dundee
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
Facility Name
Perth Royal Infirmary (Tayside NHS Trust)
City
Perth
ZIP/Postal Code
PH1 1NX
Country
United Kingdom
12. IPD Sharing Statement
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11707753
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Preventing Tolerance to Oxymetazoline in Allergic Rhinitis
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