Informationen:
Fehler:
ID
20821
Beschreibung
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
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Versionen (1)
- 20.03.17 20.03.17 -
Hochgeladen am
20. März 2017
DOI
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Lizenz
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 (End of Study Treatment)
Radium 223 Dichloride (Alpharadin) - End of Study Treatment
- StudyEvent: ODM
Ähnliche Modelle
Radium 223 Dichloride (Alpharadin) - End of Study Treatment
- StudyEvent: ODM
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
treatment period completed
Item
Did the subject complete the treatment period?
boolean
C2732579 (UMLS CUI [1])
Primary reason for discontinuation of study treatment
Item
Primary reason for discontinuation of study treatment
text
C0008976 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
C0457454 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
primary reason Adverse Event
Item
If primary reason is "Adverse Event(s) not associated with clinical disease progression", give number(s). Up to 3 AE numbers can be entered:
text
C1444662 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
primary reason Consent withdrawn
Item
If primary reason is "Withdrawal by subject (Consent withdrawn)",specify
text
C1549995 (UMLS CUI [1,1])
C1707492 (UMLS CUI [1,2])
C1707492 (UMLS CUI [1,2])
If primary reason is "Other",specify
Item
If primary reason is "Other",specify
text
C1549995 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
Subject entered active follow-up?
Item
Subject entered active follow-up?
text
C0589120 (UMLS CUI [1])