ID

20952

Description

This study is a prospective, interventional, open-label, multi-center early access program for the use of Ra-223 Cl2 in HRPC/CRPC (Hormone refractory prostate cancer / Castrate resistant prostate cancer) patients diagnosed with bone metastasis and to collect additional short and long term safety data on the product. NCT01618370

Keywords

Versions (1)
  1. 3/30/17 3/30/17 -
Uploaded on

March 30, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Radium-223 Dichloride (Alpharadin) DRKS00006460 NCT01618370 in Castration-Resistant (Hormone-Refractory) Prostate Cancer Patients With Bone Metastases (Survival Follow-up)

English

Radium 223 Dichloride (Alpharadin) - Survival Follow-up

1 forms  
Survival Assessment
Description

Survival Assessment

Date of contact
Description

dd MMM Y.Y.Y.Y

Data type

date

Alias
UMLS CUI [1]
C0805839
At this assessment was the subject alive ?
Description

lf No, complete all relevant pages.

Data type

boolean

Alias
UMLS CUI [1,1]
C2584946
UMLS CUI [1,2]
C0220825
End of Survival Follow-up
Description

End of Survival Follow-up

Primary reason for discontinuation of survival follow-up
Description

Primary reason for discontinuation

Data type

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C0457454
UMLS CUI [1,3]
C1549995
If primary reason is `Other`,specify
Description

If primary reason is `Other`,specify

Data type

text

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C0205394
If primary reason is "Death",Date of Death
Description

dd MMM Y.Y.Y.Y

Data type

date

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C1148348
Primary cause of death
Description

Primary cause of death

Data type

text

Alias
UMLS CUI [1]
C0007465
If other, specify:
Description

Other Cause of Death

Data type

text

Alias
UMLS CUI [1]
C0007465
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Similar models

Radium 223 Dichloride (Alpharadin) - Survival Follow-up

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Survival Assessment
Date of contact
Item
Date of contact
date
C0805839 (UMLS CUI [1])
At this assessment was the subject alive ?
Item
At this assessment was the subject alive ?
boolean
C2584946 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
Item Group
End of Survival Follow-up
Primary reason for discontinuation
Item
Primary reason for discontinuation of survival follow-up
text
C0008976 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
If primary reason is `Other`,specify
Item
If primary reason is `Other`,specify
text
C1549995 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
If primary reason is "Death",Date of Death
Item
If primary reason is "Death",Date of Death
date
C1549995 (UMLS CUI [1,1])
C1148348 (UMLS CUI [1,2])
Primary cause of death
Item
Primary cause of death
text
C0007465 (UMLS CUI [1])
Other Cause of Death
Item
If other, specify:
text
C0007465 (UMLS CUI [1])
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