Validation of the Rhinitis Control Scoring System (RCSS)
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Purpose
Many patients suffering from allergic rhinitis do not recognize or perceive their symptoms. Instruments have been developed to assess quality of life in rhinitis, asthma or both, but there is a need to develop validated tools or methods to assess rhinitis control among rhinitis and/or asthmatic patients. The aim of this study is to assess the discriminative and evaluative properties of the RCSS in asthmatic patients with allergic rhinitis.
| Condition | Intervention |
|---|---|
|
Asthma Rhinitis |
Drug: Mometasone furoate and desloratadine |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Validation of a Rhinitis Control Tool : the Rhinitis Control Scoring System (RCSS) |
- Discriminative (internal consistency, cross sectional construct validity and reliability) and evaluative (responsiveness and longitudinal construct validity) properties of the RCSS. [ Time Frame: March to November 2009 ] [ Designated as safety issue: No ]
- The relationship between rhinitis control and asthma control. [ Time Frame: March to November 2009 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 50 |
| Study Start Date: | March 2009 |
| Estimated Study Completion Date: | September 2012 |
| Estimated Primary Completion Date: | June 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Medication |
Drug: Mometasone furoate and desloratadine
One month treatment with both drugs
Other Names:
|
Detailed Description:
Allergic asthmatic subjects showing seasonal rhinitis symptoms will be recruited. The discriminative (internal consistency, cross sectional construct validity and reliability) and evaluative (responsiveness and longitudinal construct validity) properties of the RCSS will be evaluated as well as the relationship between rhinitis control and asthma control. RCSS will be completed at various time points during the seasonal allergic period.
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- asthma
- seasonal allergic rhinitis
Exclusion Criteria:
- smoking
- nasal polyposis
Contacts and Locations| Contact: Marie-Eve Boulay, MSc | 418-656-8711 ext 2617 | Marie-Eve.Boulay@criucpq.ulaval.ca |
| Canada, Quebec | |
| Institut universitaire de cardiologie et de pneumologie de Québec | Recruiting |
| Québec, Quebec, Canada, G1V 4G5 | |
| Contact: Marie-Eve Boulay, MSc 418-656-8711 ext 2617 Marie-Eve.Boulay@criucpq.ulaval.ca | |
| Principal Investigator: Louis-Philippe Boulet, MD | |
| Principal Investigator: | Louis-Philippe Boulet, MD | Institut universitaire de cardiologie et de pneumologie de Québec |
More Information
No publications provided
| Responsible Party: | Louis-Philippe Boulet, Professeur, Laval University |
| ClinicalTrials.gov Identifier: | NCT00967967 History of Changes |
| Other Study ID Numbers: | CER 20389 |
| Study First Received: | August 26, 2009 |
| Last Updated: | February 1, 2012 |
| Health Authority: | Canada: Canadian Institutes of Health Research |
Keywords provided by Laval University:
|
control symptoms |
Additional relevant MeSH terms:
|
Asthma Rhinitis Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases Nose Diseases Respiratory Tract Infections Otorhinolaryngologic Diseases Mometasone furoate |
Desloratadine Anti-Allergic Agents Therapeutic Uses Pharmacologic Actions Anti-Inflammatory Agents Cholinergic Antagonists Cholinergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Histamine H1 Antagonists, Non-Sedating Histamine H1 Antagonists Histamine Antagonists Histamine Agents |
ClinicalTrials.gov processed this record on May 19, 2013