GSK study: Ropinirole in RLS patients 101468/243 - Form Death

Death Form
Descrizione

Death Form

Alias
UMLS CUI-1
C1306577
Certified cause of death
Descrizione

Certified cause of death

Tipo di dati

text

Alias
UMLS CUI [1]
C3262229
Date of death
Descrizione

Date of death

Tipo di dati

date

Alias
UMLS CUI [1]
C1148348
Please complete Serious Adverse Experience section with regard to death.
Descrizione

Please complete Serious Adverse Experience section with regard to death.

Tipo di dati

text

Alias
UMLS CUI [1]
C1519255
Was an autopsy carried out?
Descrizione

If ‘Yes’ please summarize findings (include diagnosis):

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0004398
Please summarize findings of autopsy (include diagnosis):
Descrizione

Only fill in if you answered previous question with ‘Yes’.

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0004398
UMLS CUI [1,2]
C0243095
UMLS CUI [2,1]
C0004398
UMLS CUI [2,2]
C0011900
Reporting Physician’s Signature
Descrizione

Reporting Physician’s Signature

Tipo di dati

text

Alias
UMLS CUI [1]
C2346576
Reporting Physician’s Signature Date
Descrizione

Investigator signature date

Tipo di dati

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008

Similar models

GSK study: Ropinirole in RLS patients 101468/243 - Form Death

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Death Form
C1306577 (UMLS CUI-1)
Certified cause of death
Item
Certified cause of death
text
C3262229 (UMLS CUI [1])
Date of death
Item
Date of death
date
C1148348 (UMLS CUI [1])
Serious Adverse Event
Item
Please complete Serious Adverse Experience section with regard to death.
text
C1519255 (UMLS CUI [1])
autopsy
Item
Was an autopsy carried out?
boolean
C0004398 (UMLS CUI [1])
autopsy findings
Item
Please summarize findings of autopsy (include diagnosis):
text
C0004398 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
C0004398 (UMLS CUI [2,1])
C0011900 (UMLS CUI [2,2])
Reporting Physician’s Signature
Item
Reporting Physician’s Signature
text
C2346576 (UMLS CUI [1])
Investigator signature date
Item
Reporting Physician’s Signature Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])