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Detection and Characterisation of Varicella Zoster Virus From Dermal Lesions of Chickenpox-infected Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00127608
First Posted: August 8, 2005
Last Update Posted: October 12, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
GlaxoSmithKline
August 4, 2005
August 8, 2005
October 12, 2017
June 2005
July 2006   (Final data collection date for primary outcome measure)
VZV DNA per clinical sample collected
Same as current
Complete list of historical versions of study NCT00127608 on ClinicalTrials.gov Archive Site
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Detection and Characterisation of Varicella Zoster Virus From Dermal Lesions of Chickenpox-infected Patients
An Open, Prospective, Non-prophylactic, Non Therapeutic Study for the Detection and Characterisation of Varicella Zoster Virus Collected From Dermal Lesions of Patients Who Are Diagnosed of Having Varicella
This study is conducted in order to collect clinical samples from patients who are diagnosed of having chickenpox infection. The results of this study will provide basic scientific information about chickenpox disease.
The study involves NO therapeutic or prophylactic treatment nor further observation of the patients. There is no product to be tested in this study.
Interventional
Phase 3
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Chickenpox
Biological: Chickenpox infection
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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July 2006   (Final data collection date for primary outcome measure)
Pediatric patients who are diagnosed of having varicella and are presenting varicella dermal lesions.
Sexes Eligible for Study: All
up to 16 Years   (Child)
No
Contact information is only displayed when the study is recruiting subjects
Czechia
Czech Republic
 
NCT00127608
103815
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GlaxoSmithKline
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
September 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP