ID

12142

Beschrijving

An open-label, multicenter, randomized, comparative, phase III study to evaluate the efficacy and safety of rituximab plus fludarabine and cyclophosphamide (FCR) versus fludarabine and cyclophosphamide alone (FC) in previously treated patients with CD20 positive B-cell chronic lymphocytic leukemia (CLL). FCR Versus FC Alone in the Treatment of Chronic Lymphocytic Leukemia (CLL) in Relapsed Patients NCT00090051 Roche BO17072 Treatments given for an adverse event should be recorded on the appropriate “Adverse event” page. Treatments given for prophylaxis or treatment of abnormal laboratory values (e.g. blood cells, potassium supplements, etc.) should be recorded on this page. List any treatments continuing at screen or that have begun since screen (or medical procedures performed) that are not recorded on Adverse event pages.

Trefwoorden

  1. 30-09-15 30-09-15 -
  2. 28-10-15 28-10-15 -
Geüploaded op

30 september 2015

DOI

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Licentie

Creative Commons BY-NC 3.0 Legacy

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CLL Concomitant Treatments NCT00090051 BO17072

Concomitant Treatmants Chronic Lymphocytic Leukemia NCT00090051 BO17072

Concomitant treatments (or medical procedures) other than for CLL
Beschrijving

Concomitant treatments (or medical procedures) other than for CLL

Alias
UMLS CUI-1
C1707479
Treatments given for an adverse event should be recorded on the appropriate “Adverse event” page. Treatments given for prophylaxis or treatment of abnormal laboratory values (e.g. blood cells, potassium supplements, etc.) should be recorded on this page. List any treatments continuing at screen or that have begun since screen (or medical procedures performed) that are not recorded on Adverse event pages.
Beschrijving

Info

Datatype

text

Name of concomitant treatment
Beschrijving

Name of treatment

Datatype

text

Alias
UMLS CUI [1]
C1707479
Total Daily Dose of Agent (or Drug)
Beschrijving

Concomitant Medication Daily Dose

Datatype

float

Maateenheden
  • mg
Alias
UMLS CUI [1]
C2826638
mg
Start date
Beschrijving

Concomitant Medication Start Date

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2826734
dd/mm/yy
End Date
Beschrijving

Concomitant Medication End Date

Datatype

date

Maateenheden
  • dd/mm/yy
Alias
UMLS CUI [1]
C2826744
dd/mm/yy
Ongoing
Beschrijving

Concomitant Medication Ongoing

Datatype

boolean

Alias
UMLS CUI [1]
C2826666
Reason
Beschrijving

Concomitant Medication Use Reason

Datatype

text

Alias
UMLS CUI [1,1]
C0450442
UMLS CUI [1,2]
C0521115

Similar models

Concomitant Treatmants Chronic Lymphocytic Leukemia NCT00090051 BO17072

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Concomitant treatments (or medical procedures) other than for CLL
C1707479 (UMLS CUI-1)
Info
Item
Treatments given for an adverse event should be recorded on the appropriate “Adverse event” page. Treatments given for prophylaxis or treatment of abnormal laboratory values (e.g. blood cells, potassium supplements, etc.) should be recorded on this page. List any treatments continuing at screen or that have begun since screen (or medical procedures performed) that are not recorded on Adverse event pages.
text
Name of treatment
Item
Name of concomitant treatment
text
C1707479 (UMLS CUI [1])
Concomitant Medication Daily Dose
Item
Total Daily Dose of Agent (or Drug)
float
C2826638 (UMLS CUI [1])
Concomitant Medication Start Date
Item
Start date
date
C2826734 (UMLS CUI [1])
Concomitant Medication End Date
Item
End Date
date
C2826744 (UMLS CUI [1])
Concomitant Medication Ongoing
Item
Ongoing
boolean
C2826666 (UMLS CUI [1])
Concomitant Medication Use Reason
Item
Reason
text
C0450442 (UMLS CUI [1,1])
C0521115 (UMLS CUI [1,2])

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