Status:

COMPLETED

Rhinocort Aqua Versus Placebo and Fluticasone Propionate

Lead Sponsor:

AstraZeneca

Conditions:

Seasonal Allergic Rhinitis

Eligibility:

All Genders

12+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to compare once daily treatment with Rhinocort against placebo and Fluticasone Propionate at reliving the nasal symptoms of seasonal allergic rhinitis.

Eligibility Criteria

Inclusion

  • At least a 2 year documented history of seasonal allergic rhinitis
  • who, in the opinion of the investigator,
  • is a candidate for treatment with nasal steroids based on a history of either
  • a)inadequate control of symptoms with antihistamines, decongestants and/or immunotherapy, or
  • b) prior successful treatment with nasal steroids.
  • A positive response to a skin prick test at Visit 1 or within the last 12 months for grass allergens that must be present in the subject's environment for the duration of the study.

Exclusion

  • Primary or secondary adrenal insufficiency
  • Nasal candidiasis, rhinitis medicamentosa, acute or chronic sinusitis, influenza, upper respiratory tract infection or structural abnormalities of the nose (e.g., septal deviation, nasal polyps) symptomatic enough to cause significant nasal obstruction as judged by the investigator.
  • A diagnosis of asthma requiring treatment as specifies in the protocol.

Key Trial Info

Start Date :

April 1 2003

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

July 1 2003

Estimated Enrollment :

750 Patients enrolled

Trial Details

Trial ID

NCT00641680

Start Date

April 1 2003

End Date

July 1 2003

Last Update

January 24 2011

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