- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00257582
Study Of Cutaneous Disease Accompanied With Pruritus In Pediatrics
May 3, 2013 updated by: GlaxoSmithKline
Long-term Study of Cetirizine Dry Syrup in Children Suffering From Various Type of Cutaneous Disease Accompanied With Pruritus.
To assess the safety of long-term use of cetirizine dry syrup in children with various type of cutaneous disease accompanied on pruritus.
Study Overview
Study Type
Interventional
Enrollment
60
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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- GSK Investigational Site
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 year to 10 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Chronic urticaria
- Eczema & dermatitis group
- Atopic dermatitis
- Prurigo group: Acute prurigo, Prurigo subacuta, Chronic prurigo
- Pruritus cutaneous: Systemic pruritus cutaneous, Topical pruritus cutaneous
- Giving informed consent
- Children who have 2 grades or more pruritus score when assessed by the investigator or sub-investigator with the criteria for the diurnal or nocturnal pruritus score in the patient diary.
- Children with a pruritus severity of "2.Mild" or severer on the first day of the treatment period.
Exclusion criteria:
- have a history of drug hypersensitivity
- are pregnant, lactating or possibly pregnant female children.
- have asthma that requires the treatment with corticosteroid.
- cannot avoid the use of external steroid classified into "strong", "strongest" or "very strong".
- have pruritus only on face and head.
- have inappropriate complication of dermal disorder that may influence on the evaluation of the study drug.
- are undergoing specific desensitization therapy or immunomodulation therapy or phototherapy.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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To assess the safety
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Secondary Outcome Measures
Outcome Measure |
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-severity of pruritus -total pruritus score -daily main prurutus score -Severity of eruption -Patient global Improvement rating -Body temperature -Adverse events -Cetirizine serum concentrations
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2005
Study Registration Dates
First Submitted
November 21, 2005
First Submitted That Met QC Criteria
November 22, 2005
First Posted (Estimate)
November 23, 2005
Study Record Updates
Last Update Posted (Estimate)
May 6, 2013
Last Update Submitted That Met QC Criteria
May 3, 2013
Last Verified
May 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 104915
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Clinical Trials on Cetirizine Dry Syrup
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UCB Biopharma SRLCompletedHealthy Study ParticipantsJapan
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Chulalongkorn UniversityUnknown