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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00160563
Registration number
NCT00160563
Ethics application status
Date submitted
8/09/2005
Date registered
12/09/2005
Date last updated
3/03/2015
Titles & IDs
Public title
Prevention of Asthma With Levocetirizine (36 Month Treatment) in Young Children Suffering From Eczema (Atopic Dermatitis) and Sensitized to Grass Pollen and House Dust Mite and Having Completed the Previous EPAAC Trial (NCT00152464)
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Scientific title
The Prolongation of the EPAAC™ Trial - NCT00152464 (The Early Prevention of Asthma in Atopic Children). A Multi-country, Double Blind, Placebo (PLC) Controlled, Follow-up Trial With 3 Parallel Groups (LCTZ-LCTZ, LCTZ-PLC and PLC-PLC) : Evaluation of the Long Term Efficacy and Safety of Levocetirizine (LCTZ) (5 mg/ml Oral Drops -0.125 mg/kg b.w. b.i.d.) Administered for an Additional 18 Months Period in Preventing the Onset of Asthma in Children Coming From the EPAAC Trial.
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Secondary ID [1]
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A00384
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Asthma
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Condition category
Condition code
Respiratory
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Asthma
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - LEVOCETIRIZINE
Other interventions - Placebo
Experimental: LCTZ-LCTZ - Levocetirizine after having been randomized to Levocetirizine in the preceding A00309 trial - NCT00152464 (LCTZ-LCTZ)
Placebo comparator: LCTZ-PLC - Placebo after having been randomized to Levocetirizine in the preceding A00309 trial - NCT00152464 (LCTZ - PLC)
Placebo comparator: PLC-PLC - Placebo after having been randomized to Placebo in the preceding A00309 trial - NCT00152464 (PLC-PLC)
Treatment: Drugs: LEVOCETIRIZINE
5mg/mL oral drops, 0.125 mg/kg body weight, bid for 18 months
Other interventions: Placebo
Oral drops, bid for 18 months
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Intervention code [1]
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Treatment: Drugs
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Intervention code [2]
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Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Time to Onset of Asthma
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Assessment method [1]
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Timepoint [1]
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36 months (from the randomization visit to the preceding A00309 - NCT00152464 trial onwards.)
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Secondary outcome [1]
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Time to Onset of Asthma in the Subset of Subjects Still Asthma Free After First 18 Months.
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Assessment method [1]
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Timepoint [1]
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18 months (from the end of the preceding A00309 - NCT00152464 trial onwards.)
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Eligibility
Key inclusion criteria
Inclusion criteria which must be verified at the end of first 18-months treatment (Visit 9)
* Having completed the previous 18-month treatment period of the EPAAC trial - NCT00152464
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Minimum age
30
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Maximum age
42
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* None
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Stopped early
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/06/2004
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/03/2006
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Sample size
Target
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Accrual to date
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Final
207
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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- North Adelaide
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Recruitment hospital [2]
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- Parkville (North Melbourne)
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- North Adelaide
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Recruitment postcode(s) [2]
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- Parkville (North Melbourne)
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Recruitment outside Australia
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Belgium
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Bruxelles
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Czech Republic
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Brno
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Hradec Kralove
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Olomouc
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Ostrava 9
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Dorchester
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Enfield
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Southampton
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Funding & Sponsors
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Name
UCB Pharma
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Summary
Brief summary
Prolongation of the EPAAC™ trial - NCT00152464 (The Early Prevention of Asthma in Atopic Children). 36 months study to evaluate the efficacy and safety of levocetirizine (LCTZ) in preventing the onset of asthma in young atopic children.
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Trial website
https://clinicaltrials.gov/study/NCT00160563
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Trial related presentations / publications
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Contacts
Principal investigator
Name
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Isabelle Campine, MD
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Address
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UCB Pharma
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results are available at
https://clinicaltrials.gov/study/NCT00160563
Download to PDF