A Comparison of Aerius Continuous Treatment Versus Aerius PRN for Chronic Idiopathic Urticaria (Study P03147)(COMPLETED) (ATTITUD)
This study has been completed.
Information provided by:
First received: October 30, 2008
Last updated: NA
Last verified: October 2008
History: No changes posted
This double-blind pilot study was conducted to establish the best way of using desloratadine treatment to protect quality of life of chronic idiopathic urticaria (CIU) patients, after an initial 4-weeks of daily treatment: prolonging systematic daily treatment or as needed (PRN; in the case of symptoms).
Chronic Idiopathic Urticaria
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
||A Pilot, Multicenter, Double-Blind Randomized Study for Comparison of Aerius® "Continuous Treatment" Versus Aerius® "PRN Regimen" on Chronic Idiopathic Urticaria Patient Quality of Life
Primary Outcome Measures:
- Changes from Visit 2 to Visit 4 of Vq-derm questionnaire score and DLQI quality of life score. [ Time Frame: 2 months ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Estimation of disease free period after 3 months of daily treatment. [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Average usage of rescue medication [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Change from Visit 2 in pruritus symptom score assessed by the patient. [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- % of patients free of symptoms 2 months after Visit 4 [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Changes from Visit 2 of overall conditions of CIU [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Discontinuation due to treatment failure [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Investigator's assessment of response to therapy [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Quality of disease control [ Time Frame: 2 months ] [ Designated as safety issue: No ]
- Average consumption of treatment between Visit 2 and Visit 5 [ Time Frame: 4 months ] [ Designated as safety issue: No ]
| Study Start Date:
| Study Completion Date:
| Primary Completion Date:
||February 2004 (Final data collection date for primary outcome measure)
Active Comparator: Continuous Treatment
Patients received desloratadine 5 mg daily, given as one tablet in the evening, and were asked to take one tablet of "rescue medication" (Placebo) in case of symptoms for 2 months.
Experimental: PRN regimen
Patients received Placebo daily, given as one tablet in the evening, and were asked to take one tablet of "rescue medication" (desloratadine 5 mg) in case of symptoms for 2 months.
|Ages Eligible for Study:
||18 Years and older
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Subjects must demonstrate their willingness to participate in the study and comply with its procedures by signing a written informed consent.
- Subjects must be >= 18 years of age
- Women of childbearing potential must have a negative urine pregnancy test at Visit 1 (Day 1) and must be using an acceptable method of birth control during the study.
- Subjects must be in general good health; ie, they must be free of any clinically significant disease (other than CIU) that would interfere with study evaluations.
- Subjects must understand and be able to adhere to visit schedules, and agree to complete the questionnaires and a diary.
- Subjects must have at least a 6-week history of CIU (pruritus and hives) prior to Visit 1.
- Women who are pregnant or nursing.
- Subjects who used any investigational drug in the last 30 days prior to Visit 1
- Subjects with asthma requiring chronic use of inhaled or systemic corticosteroids.
- Subjects who have been treated with any investigational antibodies for asthma or allergic rhinitis in the 90 days prior to Baseline.
- Subjects who have been treated with intra-muscular or intra-articular corticosteroids in the 90 days prior to Baseline.
- Subjects with urticaria that is primarily due to physical urticaria or other known etiology, except dermographism.
- Subjects treated by immunosuppresive drugs.
- Subjects who have been hospitalized (including an emergency department visit) because of deterioration in their CIU within 3 months prior to Visit 1.
- Subjects with a history of hypersensitivity to desloratadine or any of its excipients.
- Subjects previously randomized into this study.
- Subjects who have any clinically significant metabolic, cardiovascular, immunological, neurological, hematological, gastrointestinal, cerebrovascular, or respiratory disease, or any other disorder which, in the judgment of the investigator, may interfere with the study evaluations or affect subject safety.
- Subjects with a history of psychosis, antagonistic personality, poor motivation, hypochondriasis, or any other emotional or intellectual problems that are likely to limit the validity of consent to participate in the study.
- Subjects with a history of noncompliance with medications or treatment protocols.
No Contacts or Locations Provided
No publications provided
||Head, Clinical Trials Registry & Results Disclosure Group, Schering-Plough
History of Changes
|Other Study ID Numbers:
|Study First Received:
||October 30, 2008
||October 30, 2008
||France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on December 05, 2013
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