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Title: Telemetric and Holter ECG Warehouse (THEW): Thorough QT Study #2 ECG Data      
dateReleased:
01-01-2015
description:
Study Design: This is a single-center, single-dose, randomized, double-blind, double-dummy, placebo-controlled, active-comparator, four-way crossover study. Each subject received a single dose of each of treatment (i.e., A, B, C, and D) by random assignment to one of four sequences (ABCD, BDAC, CADB, or DCBA). These treatments will be separated by a washout period of at least 7 days. The four treatments consist of the following: 1. Treatment ATherapeutic dose of RO XXXXXXX Treatment ( data not provided) 2. Treatment B:Supratherapeutic dose of RO XXXXXXX Treatment (data not provided) 3. Treatment CActive comparator Treatment - 400 mg moxifloxacin capsule 4. Treatment DPlacebo Treatment The total duration of the study is up to 9 weeks (from screening through study completion) for each enrolled subject as follows: Screening: Up to 4 weeks Dosing periods: 4 weeks (1 week washout period between each dosing) Follow-up: 7 (+3) days after last dosing (study completion) The end of the trial is defined as the date of the last visit or receipt of last data point for statistical analysis of the last subject undergoing the trial. Note: four patients have only one Holter ECG, they are the patients 2382, 4986, 6105 and 9545.
privacy:
information not available
aggregation:
instance of dataset
availability:
THEW Data Use Agreements (see Thew website for details)
refinement:
raw
ID:
handle:11614/715
types:
image
ID:
doi:10.1016/j.jelectrocard.2010.07.015
accessURL: http://thew-project.org/register_main.htm
storedIn:
CardioVascular Research Grid
format:
.ecg, .ann
accesstypes:
Landing Page
authentication:
none
authorization:
none
abbreviation:
JHU
homePage: http://www.jhu.edu/
ID:
SCR:010247
name:
Johns Hopkins University
abbreviation:
CVRG
homePage: http://www.cvrgrid.org/
ID:
SCR:004472
name:
CardioVascular Research Grid

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