ID

31176

Descrizione

Study ID: 104505 Clinical Study ID: BEX104505 Study Title: Phase II Study of Iodine 131 Anti B1 Antibody for 1st or 2nd Relapsed Indolent B-Cell Lymphomas or B-Cell Lymphomas That Have Transformed to a More Aggressive Histology Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00950755 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Keywords

  1. 25/07/18 25/07/18 -
Titolare del copyright

see clinicaltrials.gov

Caricato su

25 luglio 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Iodine 131 B1 Antibody for B-Cell Lymphomas NCT00950755

Notification of Patient Death

Administrative Data
Descrizione

Administrative Data

Alias
UMLS CUI-1
C1320722
Site Number
Descrizione

Site number

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0018704
UMLS CUI [1,2]
C0600091
Patient Number
Descrizione

Patient Number

Tipo di dati

text

Alias
UMLS CUI [1]
C1830427
Patient Initials
Descrizione

Patient Initials

Tipo di dati

text

Alias
UMLS CUI [1]
C2986440
Patient Death
Descrizione

Patient Death

Alias
UMLS CUI-1
C0011065
Date of death
Descrizione

Date of death

Tipo di dati

date

Alias
UMLS CUI [1]
C1148348
Cause of death (check one)
Descrizione

Cause of death

Tipo di dati

text

Alias
UMLS CUI [1]
C0007465
If cause of death was related to complications of treatment, please describe or reference forms on which information was recorded.
Descrizione

Complications of treatment

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0009566
Relations of study drug to patients death
Descrizione

Study drug relation to death

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C0304229
Source of information concerning death of patient (check all that apply)
Descrizione

Patient death; Source of Information

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0011065
UMLS CUI [1,2]
C1955348
UMLS CUI [1,3]
C0449416

Similar models

Notification of Patient Death

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Site number
Item
Site Number
text
C0018704 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Item Group
Patient Death
C0011065 (UMLS CUI-1)
Date of death
Item
Date of death
date
C1148348 (UMLS CUI [1])
Item
Cause of death (check one)
text
C0007465 (UMLS CUI [1])
Code List
Cause of death (check one)
CL Item
Progression of lymphoma (Progression of lymphoma)
CL Item
Complications related to drug (complete adverse Experiences form) (Complications related to drug (complete adverse Experiences form))
CL Item
Other (specify) (Other (specify))
Complications of treatment
Item
If cause of death was related to complications of treatment, please describe or reference forms on which information was recorded.
text
C0087111 (UMLS CUI [1,1])
C0009566 (UMLS CUI [1,2])
Item
Relations of study drug to patients death
text
C0011065 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Code List
Relations of study drug to patients death
CL Item
None (None)
CL Item
Remote (Remote)
CL Item
Possible (Possible)
CL Item
Probable (Probable)
Item
Source of information concerning death of patient (check all that apply)
text
C0011065 (UMLS CUI [1,1])
C1955348 (UMLS CUI [1,2])
C0449416 (UMLS CUI [1,3])
Code List
Source of information concerning death of patient (check all that apply)
CL Item
Hospital physician (Hospital physician)
CL Item
Patient's physician (Patient's physician)
CL Item
Family (Family)
CL Item
Newspaper (obituary) (Newspaper (obituary))
CL Item
Tumor registry (Tumor registry)
CL Item
Other (specify) (Other (specify))

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