ID

12349

Beschrijving

Randomized study with a run-in dose-selection phase to assess the added value of Lenalidomide in combination with standard remission-induction chemotherapy and post-remission treatment in patients aged 18-65 years with previously untreated acute myeloid leukemia (AML) or high risk myelodysplasia (MDS) (IPSS-R risk score> 4.5) Description of Form: Baseline Concomitant Diseases Form

Trefwoorden

  1. 10-11-15 10-11-15 -
  2. 23-12-15 23-12-15 -
  3. 11-02-16 11-02-16 -
Geüploaded op

10 november 2015

DOI

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Licentie

Creative Commons BY-NC 3.0

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Baseline Concomitant Diseases Form HOVON 132 AML/SAKK 30/13 EudraCT 2013-002843-26

Baseline Concomitant Diseases Form

Default Itemgroup
Beschrijving

Default Itemgroup

Alias
UMLS CUI-1
C0243087
Disease nr
Beschrijving

Disease nr

Datatype

integer

Alias
UMLS CUI [1]
C0237753
System Organ Class
Beschrijving

System Organ Class

Datatype

integer

Alias
UMLS CUI [1,1]
C2347091
UMLS CUI [1,2]
C1140263
UMLS CUI [1,3]
C1705313
UMLS CUI [1,4]
C0027365
Adverse Event Term (please use CTCAE Short Name plus Select term if applicable)
Beschrijving

Adverse Event Term

Datatype

text

Alias
UMLS CUI [1]
C2826934
Active at baseline
Beschrijving

Active at baseline

Datatype

boolean

Alias
UMLS CUI [1,1]
C0243087
UMLS CUI [1,2]
C0205177
UMLS CUI [1,3]
C1442488
CTCAE grade
Beschrijving

CTCAE grade

Datatype

float

Alias
UMLS CUI [1,1]
C1516728
UMLS CUI [1,2]
C0441800

Similar models

Baseline Concomitant Diseases Form

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Default Itemgroup
C0243087 (UMLS CUI-1)
Disease nr
Item
integer
C0237753 (UMLS CUI [1])
Item
System Organ Class
integer
C2347091 (UMLS CUI [1,1])
C1140263 (UMLS CUI [1,2])
C1705313 (UMLS CUI [1,3])
C0027365 (UMLS CUI [1,4])
Code List
System Organ Class
CL Item
Blood and lymphatic system disorders  (1)
CL Item
Cardiac disorders  (2)
CL Item
Congenital, familial and genetic disorders  (3)
CL Item
Ear and labyrinth disorders  (4)
CL Item
Endocrine disorders  (5)
CL Item
Eye disorders  (6)
CL Item
Gastrointestinal disorders  (7)
CL Item
General disorders and administration site conditions  (8)
CL Item
Hepatobiliary disorders  (9)
CL Item
Immune system disorders  (10)
CL Item
Infections and infestations  (11)
CL Item
Injury, poisoning and procedural complications  (12)
CL Item
Investigations  (13)
CL Item
Metabolism and nutrition disorders  (14)
CL Item
Musculoskeletal and connective tissue disorders  (15)
CL Item
Neoplasms benign, malignant and unspecified (incl cysts and polyps)  (16)
CL Item
Nervous system disorders  (17)
CL Item
Pregnancy, puerperium and perinatal conditions  (18)
CL Item
Psychiatric disorders  (19)
CL Item
Renal and urinary disorders  (20)
CL Item
Reproductive system and breast disorders  (21)
CL Item
Respiratory, thoracic and mediastinal disorders  (22)
CL Item
Skin and subcutaneous tissue disorders  (23)
CL Item
Social circumstances  (24)
CL Item
Surgical and medical procedures  (25)
CL Item
Vascular disorders (26)
Adverse Event Term
Item
Adverse Event Term (please use CTCAE Short Name plus Select term if applicable)
text
C2826934 (UMLS CUI [1])
Active at baseline
Item
boolean
C0243087 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,3])
CTCAE grade
Item
CTCAE grade
float
C1516728 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])

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