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Part 2: Repeat Dose Phase - Day 26 - Clinical Chemistry Result

1 Formulär  
Administrative data
Beskrivning

Administrative data

Subject Identifier
Beskrivning

Subject Identifier

Datatyp

integer

24HR Local Laboratory Result Data
Beskrivning

24HR Local Laboratory Result Data

Date sample taken
Beskrivning

Date sample taken

Datatyp

date

Time sample taken
Beskrivning

Time sample taken

Datatyp

time

Has the subject fasted?
Beskrivning

Has the subject fasted?

Datatyp

boolean

Clinical Chemistry Test
Beskrivning

Clinical Chemistry Test

TSH
Beskrivning

TSH

Datatyp

float

Måttenheter
  • U/ml
U/ml
T4
Beskrivning

T4

Datatyp

float

Måttenheter
  • g/dL
g/dL
Triglycerides
Beskrivning

Triglycerides

Datatyp

float

HDL
Beskrivning

HDL

Datatyp

float

Måttenheter
  • mg/dL
mg/dL
Calculated LDL
Beskrivning

Calculated LDL

Datatyp

float

Måttenheter
  • mmol/L
mmol/L
Total Cholesterol
Beskrivning

Total Cholesterol

Datatyp

float

If the laboratory results meet the protocol definition of an adverse evnt, record the details an the NON-Serious Adverse Events page or Serious Adverse Event page.
Beskrivning

If the laboratory results meet the protocol definition of an adverse evnt, record the details an the NON-Serious Adverse Events page or Serious Adverse Event page.

Datatyp

text

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Similar models

Part 2: Repeat Dose Phase - Day 26 - Clinical Chemistry Result

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative data
Subject Identifier
Item
Subject Identifier
integer
Item Group
24HR Local Laboratory Result Data
Date sample taken
Item
Date sample taken
date
Time sample taken
Item
Time sample taken
time
Has the subject fasted?
Item
Has the subject fasted?
boolean
Item Group
Clinical Chemistry Test
TSH
Item
TSH
float
T4
Item
T4
float
Triglycerides
Item
Triglycerides
float
HDL
Item
HDL
float
Calculated LDL
Item
Calculated LDL
float
Total Cholesterol
Item
Total Cholesterol
float
If the laboratory results meet the protocol definition of an adverse evnt, record the details an the NON-Serious Adverse Events page or Serious Adverse Event page.
Item
If the laboratory results meet the protocol definition of an adverse evnt, record the details an the NON-Serious Adverse Events page or Serious Adverse Event page.
text
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