search
Back to results

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Withdrawn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
Brian J Lipworth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Allergic Rhinitis focused on measuring allergic rhinitis, rhinitis medicamentosa, imidazolines, corticosteroid

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
February 17, 2009
Last Updated
October 24, 2016
Sponsor
Brian J Lipworth
search

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
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

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

Citations:
PubMed Identifier
11707753
Citation
Bousquet J, Van Cauwenberge P, Khaltaev N; Aria Workshop Group; World Health Organization. Allergic rhinitis and its impact on asthma. J Allergy Clin Immunol. 2001 Nov;108(5 Suppl):S147-334. doi: 10.1067/mai.2001.118891. No abstract available.
Results Reference
background
PubMed Identifier
17265594
Citation
Nassef M, Shapiro G, Casale TB; Respiratory and Allergic Disease Foundation. Identifying and managing rhinitis and its subtypes: allergic and nonallergic components--a consensus report and materials from the Respiratory and Allergic Disease Foundation. Curr Med Res Opin. 2006 Dec;22(12):2541-8. doi: 10.1185/030079906x158057.
Results Reference
background
PubMed Identifier
16005621
Citation
Nolte H, Nepper-Christensen S, Backer V. Unawareness and undertreatment of asthma and allergic rhinitis in a general population. Respir Med. 2006 Feb;100(2):354-62. doi: 10.1016/j.rmed.2005.05.012. Epub 2005 Jul 11.
Results Reference
background
PubMed Identifier
15080802
Citation
Gupta R, Sheikh A, Strachan DP, Anderson HR. Burden of allergic disease in the UK: secondary analyses of national databases. Clin Exp Allergy. 2004 Apr;34(4):520-6. doi: 10.1111/j.1365-2222.2004.1935.x.
Results Reference
background
PubMed Identifier
15138430
Citation
Ferguson BJ. Influences of allergic rhinitis on sleep. Otolaryngol Head Neck Surg. 2004 May;130(5):617-29. doi: 10.1016/j.otohns.2004.02.001.
Results Reference
background
PubMed Identifier
16911353
Citation
Patou J, De Smedt H, van Cauwenberge P, Bachert C. Pathophysiology of nasal obstruction and meta-analysis of early and late effects of levocetirizine. Clin Exp Allergy. 2006 Aug;36(8):972-81. doi: 10.1111/j.1365-2222.2006.02544.x.
Results Reference
background
PubMed Identifier
8739860
Citation
Graf P. Long-term use of oxy- and xylometazoline nasal sprays induces rebound swelling, tolerance, and nasal hyperreactivity. Rhinology. 1996 Mar;34(1):9-13.
Results Reference
background
PubMed Identifier
16784007
Citation
Ramey JT, Bailen E, Lockey RF. Rhinitis medicamentosa. J Investig Allergol Clin Immunol. 2006;16(3):148-55.
Results Reference
background
PubMed Identifier
6171024
Citation
Petruson B. Treatment with xylometazoline (Otrivin) nosedrops over a six-week period. Rhinology. 1981 Sep;19(3):167-72.
Results Reference
background
PubMed Identifier
9001263
Citation
Yoo JK, Seikaly H, Calhoun KH. Extended use of topical nasal decongestants. Laryngoscope. 1997 Jan;107(1):40-3. doi: 10.1097/00005537-199701000-00010.
Results Reference
background
PubMed Identifier
14579657
Citation
Watanabe H, Foo TH, Djazaeri B, Duncombe P, Mackay IS, Durham SR. Oxymetazoline nasal spray three times daily for four weeks in normal subjects is not associated with rebound congestion or tachyphylaxis. Rhinology. 2003 Sep;41(3):167-74.
Results Reference
background
PubMed Identifier
9179430
Citation
Hallen H, Enerdal J, Graf P. Fluticasone propionate nasal spray is more effective and has a faster onset of action than placebo in treatment of rhinitis medicamentosa. Clin Exp Allergy. 1997 May;27(5):552-8.
Results Reference
background
PubMed Identifier
9230722
Citation
Tan KS, Grove A, McLean A, Gnosspelius Y, Hall IP, Lipworth BJ. Systemic corticosteriod rapidly reverses bronchodilator subsensitivity induced by formoterol in asthmatic patients. Am J Respir Crit Care Med. 1997 Jul;156(1):28-35. doi: 10.1164/ajrccm.156.1.9610113.
Results Reference
background
PubMed Identifier
7631772
Citation
Hamamdzic D, Duzic E, Sherlock JD, Lanier SM. Regulation of alpha 2-adrenergic receptor expression and signaling in pancreatic beta-cells. Am J Physiol. 1995 Jul;269(1 Pt 1):E162-71. doi: 10.1152/ajpendo.1995.269.1.E162.
Results Reference
background
PubMed Identifier
6324653
Citation
Davies AO, Lefkowitz RJ. Regulation of beta-adrenergic receptors by steroid hormones. Annu Rev Physiol. 1984;46:119-30. doi: 10.1146/annurev.ph.46.030184.001003. No abstract available.
Results Reference
background

Learn more about this trial

Preventing Tolerance to Oxymetazoline in Allergic Rhinitis

We'll reach out to this number within 24 hrs