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Visit 1A Events PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 moduli  
Events
Descrizione

Events

Alias
UMLS CUI-1
C0877248
1. Has the patient experienced any of the following since randomization:
Descrizione

Patient experience

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0596545
UMLS CUI [1,2]
C0030705
Dizziness or Lightheadedness
Descrizione

Dizziness or Lightheadedness

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0012833
UMLS CUI [2]
C0220870
Fainting
Descrizione

Fainting

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0039070
Headache during first week of study drug administration
Descrizione

Headache

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018681
If headache occurred please indicate how it was treated (indicate all that apply):
Descrizione

If headache

Tipo di dati

integer

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C3146298
2. Have any Outcome Events or Serious Adverse Events been experienced? (See instructions on facing page)
Descrizione

Outcome Events or Serious Adverse Events

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1705586
UMLS CUI [2]
C0877248
if "Yes" please indicate all that apply
Descrizione

If Yes

Tipo di dati

integer

Alias
UMLS CUI [1]
C2348235
Please complete the respective forms
Descrizione

Please complete the respective forms

4. Signature of Investigator or Sub-Investigator
Descrizione

By signing and dating this page, I declare that I have reviewed for accuracy all the case report form pages for this patient visit; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed on the specified dates.

Tipo di dati

text

Alias
UMLS CUI [1]
C2346576
Date of Signature (dd mon yy)
Descrizione

Date of Signature

Tipo di dati

date

Alias
UMLS CUI [1,1]
C1519316
UMLS CUI [1,2]
C0011008
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Similar models

Visit 1A Events PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Events
C0877248 (UMLS CUI-1)
Patient experience
Item
1. Has the patient experienced any of the following since randomization:
text
C0596545 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Dizziness or Lightheadedness
Item
Dizziness or Lightheadedness
boolean
C0012833 (UMLS CUI [1])
C0220870 (UMLS CUI [2])
Fainting
Item
Fainting
boolean
C0039070 (UMLS CUI [1])
Headache
Item
Headache during first week of study drug administration
boolean
C0018681 (UMLS CUI [1])
Item
If headache occurred please indicate how it was treated (indicate all that apply):
integer
C0087111 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
If headache
Code List
If headache occurred please indicate how it was treated (indicate all that apply):
CL Item
Analgestic (1)
CL Item
Down titration of study medication A (2)
CL Item
No treatment (3)
Outcome Events or Serious Adverse Events
Item
2. Have any Outcome Events or Serious Adverse Events been experienced? (See instructions on facing page)
boolean
C1705586 (UMLS CUI [1])
C0877248 (UMLS CUI [2])
Item
if "Yes" please indicate all that apply
integer
C2348235 (UMLS CUI [1])
If Yes
Code List
if "Yes" please indicate all that apply
CL Item
Stroke (1)
CL Item
Myocardial Infarction (2)
CL Item
Death (3)
CL Item
New or worsening congestive heart failure (CHF) (4)
CL Item
Other designated vascular event (5)
CL Item
Hemorrhagic Event (6)
CL Item
Thrombotic Thrombocytopenia purpura (7)
CL Item
Neutropenia (8)
CL Item
Newly diagnosed diabetes (9)
Item Group
Please complete the respective forms
Signature of Investigator or Sub-Investigator
Item
4. Signature of Investigator or Sub-Investigator
text
C2346576 (UMLS CUI [1])
Date of Signature
Item
Date of Signature (dd mon yy)
date
C1519316 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
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