CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 36 enrolled
Drug / intervention
Collection of clinical samplesprocedure
Likely dose
Not stated in record
Key inclusion· 2
  • Pediatric patients diagnosed with varicella
  • Presenting with varicella dermal lesions
Key exclusion· 0

None specified.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00127608
NCT00127608Phase 3Completed

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/Breakthrough Varicella

GlaxoSmithKline·interventional·Posted Aug 8, 2005·Updated Feb 4, 2019

In Brief

A Phase 3 clinical trial evaluating Collection of clinical samples for Varicella. Completed, enrolled 36 participants across 1 site.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVaricella
CountriesCzechia
Collaborators--

Timeline

Phase 3CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedAug 8, 2005
Enrollment StartJun 7, 2005
Primary CompletionJul 13, 2006
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 20.9 years ago

Interventions

Collection of clinical samplesprocedure

The following samples were obtained from each subject: * Vesicle fluid (VF) and vesicle swabs (VS) from four vesicles (for a total of eight samples) * Papule swabs (PS) from four papules * Crusts from two lesions * One throat swab (TS) Up to 15 samples were to be obtained for each subject, when possible. VFs, VSs, PSs, and crusts were either stored dry or in liquid medium. TS samples were stored in liquid medium. After extraction of DNA, samples were tested for the presence of varicella virus using a Quantitative Polymerase Chain Reaction (Q-PCR) technique.