An Investigation to Evaluate the Technique of MRI as an Assessment of the Effect of Anti-allergy Drug Treatment on Internal Nasal and Sinus Mucosal Anatomy Following Intranasal Allergen Challenge in Subjects With Seasonal Allergic Rhinitis.

GlaxoSmithKline1 site in 1 country21 target enrollmentMarch 2007

ConditionsSeasonal Allergic Rhinitis Sinusitis

Drugspseudoephedrine hydrochloride cetirizine hydrochloride

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Seasonal Allergic Rhinitis
Sponsor: GlaxoSmithKline
Enrollment: 21
Locations: 1
Primary Endpoint: Cross-sectional airspace area (and thus also airspace volume) of the nasal passages
Status: Completed
Last Updated: 12 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this study is to establish whether MRI scanning is a sensitive measure of the effects of existing drug treatments on nasal dimensions following challenge with intranasal allergen in subjects with hayfever. If successful this technique could be applied to increase confidence for internal decision making and ultimately may be used to assess how effective a new drug treatment is.

Registry

clinicaltrials.gov

Start Date

March 2007

End Date

April 2007

Last Updated

12 years ago

Study Type

Observational

Sex

All

Investigators

Sponsor

GlaxoSmithKline

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•A medically diagnosed hay fever patient who is otherwise healthy.
•Aged 18 to 60 years.
•Body mass index less than 30 kg/m² with weight range of 50kg (females 45kg) to 100kg.
•A positive skin prick test (wheal = 3mm) for grass pollen at or within 12 months of starting the study and/or a positive RAST (= class 2) for grass pollen at or within 12 months of starting the study.
•Baseline FEV1 = 80% predicted and a baseline FEV1/FVC = 70% predicted (using standard predicted guidelines).
•Capable of giving informed consent which includes compliance with the requirements and restrictions listed in the consent form.
•Available to complete all study measurements.

Exclusion Criteria

•Pregnant or nursing females.
•Women of childbearing potential who are unwilling or unable to use an appropriate method of contraception.
•On examination the subject is found to have any nasal abnormalities or nasal polyposis, a history of frequent nosebleeds, or nasopharyngeal surgery.
•Recent (within 3 weeks) or ongoing chest infection which in the physician responsible opinion renders the subject unsuitable for participation in the study.
•The subject has a history or current evidence of perennial rhinitis, sinusitis, or any other condition potentially or directly involving the nasal cavity, sinuses or nasopharynx.
•A history of any medical condition that would not allow the use of pseudoephedrine (e.g. hypertension, diabetes mellitus, ischaemic heart disease, raised intraocular pressure, hyperthyroidism, benign prostatic hyperplasia) or cetirizine (eg. antihistamine hypersensitivity).
•Any respiratory disease other than mild stable asthma that is controlled with occasional use of as-needed short-acting beta-agonists and associated with normal lung function.
•The subject is likely to be unable to abstain from salbutamol use for 8 hours before a challenge.
•The subject has a history of drug or other allergy that, in the opinion of the physician responsible, contraindicates their participation.
•The subject has participated in another study during the previous 3 months.

Outcomes

Primary Outcomes

Cross-sectional airspace area (and thus also airspace volume) of the nasal passages

Time Frame: at 1hr post-dose and 30-60mins post-allergen challenge.

Secondary Outcomes

Volume of fluid identified adjacent to the airspace. Mucosal surface area. Nasal cavity volume. Nasal tissue volume derived from the nasal cavity volume less airspace and fluid volumes.(At 1hr post-dose and 30-60mins post-allergen challenge)