ID
32945
Description
Study ID: 107085 Clinical Study ID: GLP107085 Study Title: A Randomized, Double-blind, Parallel, Nested Crossover Study to Investigate the Effect of Albiglutide on Cardiac Repolarization (corrected QT Interval) Compared With Placebo in Healthy Male and Female Subjects: A Thorough ECG Study Employing Placebo, Albiglutide, and a Positive Control (Moxifloxacin) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01406262 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2
Keywords
Versions (1)
- 11/21/18 11/21/18 -
Copyright Holder
GSK group of companies
Uploaded on
November 21, 2018
DOI
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License
Creative Commons BY-NC 3.0
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The Effect of Albiglutide on Cardiac Repolarisation Compared with Placebo 107085
Pregnancy Outcome Form
- StudyEvent: ODM
Description
Demography
Description
Subject ID Number
Data type
integer
Description
Age
Data type
integer
Measurement units
- years
Description
Date of Birth
Data type
date
Description
Weight (kilogram)
Data type
float
Measurement units
- kg
Description
Weight (pounds)
Data type
float
Measurement units
- pounds
Description
Height (centimeters)
Data type
float
Measurement units
- cm
Description
Height (inches)
Data type
float
Measurement units
- inches
Description
Race
Data type
text
Description
Child Information
Description
Baby Number
Data type
integer
Description
Sex
Data type
text
Description
Height (centimeters)
Data type
float
Measurement units
- cm
Description
Height (inches)
Data type
float
Measurement units
- inches
Description
Weight (kilograms)
Data type
float
Measurement units
- kg
Description
Weight (pounds)
Data type
float
Measurement units
- lbs/oz
Description
Apgar score 1 min
Data type
integer
Description
Apgar score 5 min
Data type
integer
Description
Outcome of pregnancy
Data type
text
Description
If Spontaneous or Elective abortion, record the date
Data type
date
Description
if Abnormal baby, congenital abnormality, stillborn, died at birth
Data type
text
Description
Date of congenital abnormality identified/diagnosed
Data type
date
Description
Pregnancy Outcome Information
Description
Baby number
Data type
integer
Description
Date of delivery
Data type
date
Description
Length of gestation (weeks)
Data type
integer
Description
select one
Data type
text
Description
include live and stillbirth; if none, enter a zero
Data type
integer
Description
Comments
Data type
text
Description
Important Note
Description
If pregnancy outcome is serious (spontaneous abortion, congenital abnormality, stillbirth, prolonged hospitalization, etc.) please submit the SAE report.
Data type
text
Similar models
Pregnancy Outcome Form
- StudyEvent: ODM