ID

31378

Beschrijving

Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Trefwoorden

Versies (2)
  1. 24-07-18 24-07-18 -
  2. 18-08-18 18-08-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

18 augustus 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

Engels

Patient Withdrawal from Study

1 Formulieren  
Date of withdrawal from study
Beschrijving

Date of withdrawal from study

Alias
UMLS CUI-1
C0422727
UMLS CUI-2
C0011008
Date of withdrawal from study
Beschrijving

Patient withdrawn from trial; Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0011008
Reason for withdrawal from study
Beschrijving

Reason for withdrawal from study

Alias
UMLS CUI-1
C0422727
UMLS CUI-2
C3146298
Reason for withdrawal from study (check primary reason only)
Beschrijving

Patient withdrawn from trial | Indication

Datatype

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C3146298
If patient was lost to follow-up, date of last contact
Beschrijving

Lost to Follow-Up | Date last contact

Datatype

date

Alias
UMLS CUI [1]
C1302313
UMLS CUI [2]
C0805839
If other reason for withdrawal from study, please specify
Beschrijving

Patient withdrawn from trial; Indication; Other; Specification

Datatype

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C2348235
Explanation of withdrawal
Beschrijving

Explanation of withdrawal

Alias
UMLS CUI-1
C0422727
UMLS CUI-2
C0681841
Explanation of withdrawal (when appropriate)
Beschrijving

Patient withdrawn from trial; explanation

Datatype

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0681841
Terug naar het begin van de pagina

Similar models

Patient Withdrawal from Study

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Date of withdrawal from study
C0422727 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
Patient withdrawn from trial; Date in time
Item
Date of withdrawal from study
date
C0422727 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Reason for withdrawal from study
C0422727 (UMLS CUI-1)
C3146298 (UMLS CUI-2)
Item
Reason for withdrawal from study (check primary reason only)
text
C0422727 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
Patient withdrawn from trial | Indication
Code List
Reason for withdrawal from study (check primary reason only)
CL Item
Patient was lost to follow-up (explain below) (1)
CL Item
Patient wished to withdraw from study (explain below) (2)
CL Item
Patient received alternative therapy (explain below) (3)
CL Item
Patient had progressive disease (4)
CL Item
Patient died (5)
CL Item
Other (6)
Lost to Follow-Up | Date last contact
Item
If patient was lost to follow-up, date of last contact
date
C1302313 (UMLS CUI [1])
C0805839 (UMLS CUI [2])
Patient withdrawn from trial; Indication; Other; Specification
Item
If other reason for withdrawal from study, please specify
text
C0422727 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Item Group
Explanation of withdrawal
C0422727 (UMLS CUI-1)
C0681841 (UMLS CUI-2)
Patient withdrawn from trial; explanation
Item
Explanation of withdrawal (when appropriate)
text
C0422727 (UMLS CUI [1,1])
C0681841 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

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