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Azelastine Fluticasone Combination vs. Fluticasone

Primary Purpose

Allergic Rhinitis

Status
Withdrawn
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Azelastine , fluticasone
Fluticasone propionate
Sponsored by
University of Dundee
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Allergic Rhinitis focused on measuring Allergic Rhinitis

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 at least one allergen on SPT.
  • 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
  • Perth Royal Infirmary

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Azelastine Fluticasone

Fluticasone propionate

Arm Description

Outcomes

Primary Outcome Measures

Maximum percentage fall in PNIF after 400mg/ml of AMP nasal challenge between both groups.

Secondary Outcome Measures

60 minute recovery to AMP challenge
Mini RQLQ
Global visual analogue scale
Nasal lavage for cytokines
Overnight urinary cortisol creatinine ratio
Domiciliary diary cards

Full Information

First Posted
February 17, 2009
Last Updated
June 11, 2012
Sponsor
University of Dundee
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1. Study Identification

Unique Protocol Identification Number
NCT00845598
Brief Title
Azelastine Fluticasone Combination vs. Fluticasone
Official Title
A Proof of Concept Study to Evaluate Comparative Efficacy of an Azelastine/Fluticasone Combination Nasal Spray vs. Twice the Dose of Fluticasone in Persistent Allergic Rhinitis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Withdrawn
Why Stopped
Could not get IMP
Study Start Date
August 2010 (undefined)
Primary Completion Date
August 2011 (Anticipated)
Study Completion Date
August 2011 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Dundee

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to see how a combination spray of azelastine and fluticasone (antihistamine and steroid) compares with a steroid nasal spray (fluticasone) alone in allergic rhinitis i.e. does azelastine permit the use of lesser steroid dose (steroid sparing effect) to achieve the same benefit.
Detailed Description
Allergic rhinitis (AR) is a major chronic respiratory disease with a prevalence approaching nearly 25% in the worldwide population.Allergic Rhinitis is a common and relatively undiagnosed public health problem and has been reported as being one of the ten most common causes for outpatient attendances to the general practitioner. Long term untreated allergic rhinitis may lead on to asthma. When exposed to allergens (pollen, house dust mite etc) in the atmosphere, the mast cells in the nose burst and an inflammatory response is triggered and patients experience sneezing, itching, blocked nose and running. These allergens may be used as provocation agents to recreate the disease symptoms to confirm the diagnosis of which allergens one is allergic to. However, there is a risk of allergic reactions in doing so. Adenosine monophosphate (AMP)achieves the same goal by stimulating the mast cells and causing them to burst without actually the risks of allergen provocation tests. Such tests are now commonplace in research and clinical medicine. Nasal steroids are considered to be the most potent medications for allergic rhinitis, particularly nasal blockage. Nasal antihistamines are also available but they act mainly to limit nasal running, itching and sneezing and have lesser effect on blockage. The other advantage is that they act very quickly while steroids take at least 72 hours to begin acting and weeks to achieve maximal benefit. Finally, they are free of significant short and long term side effects. Having said that nasal steroids are very safe and unlike inhaled or oral steroids have not been shown to cause systemic side effects in adults. Therefore, it is interesting to see if a combination of an antihistamine and nasal steroid would add their good qualities mentioned above and by the act of reducing the dose of steroid reduce their side effects. To do this we will use nasal AMP challenge as an outcome measure as we have done research studies for over a decade with. We will look at noninvasive nasal airflow parameters, nasal nitric oxide levels, and for safety we will look at the overnight urinary cortisol and creatinine ratio which is the most sensitive and noninvasive test of urine to quantify how much steroid has been absorbed in the blood stream.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis
Keywords
Allergic Rhinitis

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
Azelastine Fluticasone
Arm Type
Experimental
Arm Title
Fluticasone propionate
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Azelastine , fluticasone
Intervention Description
Azelastine Hydrochloride BP 0.10% w/v AND Fluticasone propionate BP 0.0357% w/v as combination 1 squirt in each nostril twice daily
Intervention Type
Drug
Intervention Name(s)
Fluticasone propionate
Intervention Description
Fluticasone propionate 0.05% w/w 2 squirts in each nostril (50 μg per squirt)
Primary Outcome Measure Information:
Title
Maximum percentage fall in PNIF after 400mg/ml of AMP nasal challenge between both groups.
Time Frame
0, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Secondary Outcome Measure Information:
Title
60 minute recovery to AMP challenge
Time Frame
0, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
Mini RQLQ
Time Frame
0, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
Global visual analogue scale
Time Frame
0, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
Nasal lavage for cytokines
Time Frame
0, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
Overnight urinary cortisol creatinine ratio
Time Frame
0, 2 weeks, 4 weeks, 6 weeks, 8 weeks
Title
Domiciliary diary cards
Time Frame
2 week treatment periods

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 at least one allergen on SPT. 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
Sriram Vaidyanathan, MBBS
Organizational Affiliation
University of Dundee
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Brian Lipworth, MD, FRCP
Organizational Affiliation
University of Dundee
Official's Role
Study Director
Facility Information:
Facility Name
Ninewells Hospital and Medical School
City
Dundee
ZIP/Postal Code
DD1 9SY
Country
United Kingdom
Facility Name
Perth Royal Infirmary
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
9848901
Citation
Weiner JM, Abramson MJ, Puy RM. Intranasal corticosteroids versus oral H1 receptor antagonists in allergic rhinitis: systematic review of randomised controlled trials. BMJ. 1998 Dec 12;317(7173):1624-9. doi: 10.1136/bmj.317.7173.1624.
Results Reference
background
PubMed Identifier
7908778
Citation
Meltzer EO, Weiler JM, Dockhorn RJ, Widlitz MD, Freitag JJ. Azelastine nasal spray in the management of seasonal allergic rhinitis. Ann Allergy. 1994 Apr;72(4):354-9.
Results Reference
background
PubMed Identifier
9195148
Citation
Newson-Smith G, Powell M, Baehre M, Garnham SP, MacMahon MT. A placebo controlled study comparing the efficacy of intranasal azelastine and beclomethasone in the treatment of seasonal allergic rhinitis. Eur Arch Otorhinolaryngol. 1997;254(5):236-41. doi: 10.1007/BF00874095.
Results Reference
background
PubMed Identifier
10400480
Citation
Berger WE, Fineman SM, Lieberman P, Miles RM. Double-blind trials of azelastine nasal spray monotherapy versus combination therapy with loratadine tablets and beclomethasone nasal spray in patients with seasonal allergic rhinitis. Rhinitis Study Groups. Ann Allergy Asthma Immunol. 1999 Jun;82(6):535-41. doi: 10.1016/s1081-1206(10)63161-4.
Results Reference
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Azelastine Fluticasone Combination vs. Fluticasone

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