ISRCTN23032971CompletedNot Applicable
Morning versus evening dosing of desloratadine in seasonal allergic rhinitis: a randomised controlled study
Schering-Plough AS (Norway)0 sites663 target enrollmentStarted: February 1, 2005Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 663
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1. Patients 18 years or above with a minimum of two years history of SAR confirmed by either a positive skin prick test or a positive serologic allergen test to the relevant seasonal allergen
- •2. Clinically symptomatic with SAR at baseline/inclusion with a minimum total nasal symptom score (rhinorrhoea, congestion, itching and sneezing) of at least 6 and rhinorrhoea being minimum 2 (moderate)
- •3. Willingness to adhere to dosing and visit schedule
- •4. Females of childbearing potential have to use medically accepted methods of birth control
- •5. Written informed consent
Exclusion Criteria
- •1. Pulmonary disease, perennial rhinitis, sinusitis, rhinitis medicamentosa, pollen desensitisation during the last 6 months
- •2. Respiratory tract infection within the last two weeks
- •3. Structural nasal abnormalities (including polyps)
- •4. Use of oral, nasal, ocular decongestants, corticosteroids in any form (except mild dermatological group I corticosteroids allowed in only small areas), other antihistamines (oral or topical), any investigational drug during the last 30 days
- •5. Pregnant or nursing females
Investigators
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