ID

5312

Beschrijving

Prospective non–randomized multi​center study for epidemiology and characterization of Myelodysplastic Syndromes(MDS) and Juvenile Myelomonocytic Leukemia (JMML) in child­hood. PI: Prof. Dr. Charlotte Niemeyer http://clinicaltrials.gov/ct2/show/NCT00662090 http://www.ewog-mds.org/

Link

http://clinicaltrials.gov/ct2/show/NCT00662090

Trefwoorden

  1. 05-08-14 05-08-14 - Martin Dugas
  2. 05-08-14 05-08-14 - Martin Dugas
Geüploaded op

5 augustus 2014

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

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EWOG MDS 2006 Previous history DRKS00003789

Previous history

  1. StudyEvent: SE
    1. Previous history
Show identification of patient
Beschrijving

Show identification of patient

Dummy
Beschrijving

Dummy

Datatype

text

Previous history
Beschrijving

Previous history

Xanthoma
Beschrijving

Xanthoma

Datatype

integer

Café-au-lait spots
Beschrijving

Café-au-lait spots

Datatype

integer

Other symptoms of NF1
Beschrijving

Other symptoms of NF1

Datatype

integer

1° relatives with NF1
Beschrijving

1° relatives with NF1

Datatype

integer

Previous congenital bone marrow failure disorder
Beschrijving

Previous congenital bone marrow failure disorder

Datatype

integer

Previous acquired bone marrow failure disorder
Beschrijving

Previous acquired bone marrow failure disorder

Datatype

integer

Previous malignancy
Beschrijving

Previous malignancy

Datatype

integer

Previous chemo-radiotherapy (CT and/or RT)
Beschrijving

Previous chemo-radiotherapy (CT and/or RT)

Datatype

integer

Mental retardation
Beschrijving

Mental retardation

Datatype

integer

Birth weight < third percentile
Beschrijving

Birth weight < third percentile

Datatype

integer

Height < third percentile (at diagnosis)
Beschrijving

Height < third percentile (at diagnosis)

Datatype

integer

Weight < third percentile (at diagnosis)
Beschrijving

Weight < third percentile (at diagnosis)

Datatype

integer

Head circumference < third percentile (at diagnosis)
Beschrijving

Head circumference < third percentile (at diagnosis)

Datatype

integer

Clinical evidence of PNH
Beschrijving

Clinical evidence of PNH

Datatype

integer

Hepatitis/Hepatopathy
Beschrijving

Hepatitis/Hepatopathy

Datatype

integer

Patient is twin
Beschrijving

Patient is twin

Datatype

integer

Congenital abnormalities
Beschrijving

Congenital abnormalities

Datatype

integer

Other abnormalities
Beschrijving

Other abnormalities

Datatype

integer

Number of cafe au lait spots
Beschrijving

Number of cafe au lait spots

Number of Café-au-lait spots
Beschrijving

Number of Café-au-lait spots

Datatype

integer

Type of other NF1 Symptoms
Beschrijving

Type of other NF1 Symptoms

Neurofibroma of any type
Beschrijving

Neurofibromas of any type

Datatype

integer

Plexiform neurofibroma
Beschrijving

Plexiform neurofibroma

Datatype

integer

Freckling in the axillary or inguinal regions
Beschrijving

Freckling in the axillary or inguinal regions

Datatype

integer

Optic glioma
Beschrijving

Optic glioma

Datatype

integer

>= 2 Lisch nodules of the iris
Beschrijving

>= 2 Lisch nodules of the iris

Datatype

integer

Osseous lesions associated with NF1
Beschrijving

Osseous lesions associated with NF1

Datatype

integer

Degree of relationship of NF1 relatives
Beschrijving

Degree of relationship of NF1 relatives

Mother
Beschrijving

Mother

Datatype

integer

Father
Beschrijving

Father

Datatype

integer

Sister
Beschrijving

Sister

Datatype

integer

Brother
Beschrijving

Brother

Datatype

integer

Other relatives
Beschrijving

Other relatives

Datatype

integer

Type of previous cBMF
Beschrijving

Type of previous cBMF

Previous congenital bone marrow failure disorder
Beschrijving

Previous congenital bone marrow failure disorder

Datatype

integer

Other type of congenital BMF
Beschrijving

Type

Datatype

text

Date and type of acquired BMF
Beschrijving

Date and type of acquired BMF

Date of previous aBMF
Beschrijving

Date of previous aBMF

Datatype

date

Type of aBMF
Beschrijving

Previous acquired bone marrow failure disorder

Datatype

integer

Other type of aBMF
Beschrijving

Previous acquired bone marrow failure disorder

Datatype

text

Date and type of previous malignancy
Beschrijving

Date and type of previous malignancy

Date of previous malignancy
Beschrijving

Date of previous malignancy

Datatype

date

Type of previous malignancy
Beschrijving

Type of previous malignancy

Datatype

integer

Other type of previous malignancy
Beschrijving

Other type of previous malignancy

Datatype

text

Type of previous chemo therapy
Beschrijving

Type of previous chemo therapy

Type of chemo therapy
Beschrijving

Type of chemo therapy

Datatype

text

Type of radiotherapy
Beschrijving

Type of radiotherapy

Datatype

text

Type of cong. abnormalities
Beschrijving

Type of cong. abnormalities

Type of congenital abnormalities
Beschrijving

Type of congenital abnormalities

Datatype

text

Type of other abnormalties
Beschrijving

Type of other abnormalties

Type of other abnormalities
Beschrijving

Type of other abnormalities

Datatype

text

Type of twin
Beschrijving

Type of twin

Type of twin
Beschrijving

Type of twin

Datatype

integer

Family history
Beschrijving

Family history

Parents are consanguineous
Beschrijving

Parents are consanguineous

Datatype

integer

History of malignancies in family (1° relatives)
Beschrijving

History of malignancies in family (1° relatives)

Datatype

integer

History of hemato-/immunological diseases
Beschrijving

History of hemato-/immunological diseases

Datatype

integer

History of other possibly relevant diseases
Beschrijving

History of other possibly relevant diseases

Datatype

integer

Family history of malignancies
Beschrijving

Family history of malignancies

Mother
Beschrijving

Mother

Datatype

integer

Father
Beschrijving

Father

Datatype

integer

Sister
Beschrijving

Sister

Datatype

integer

Brother
Beschrijving

Brother

Datatype

integer

Mother affected
Beschrijving

Mother affected

Type of mother's malignancy
Beschrijving

Type of mother's malignancy

Datatype

text

Father affected
Beschrijving

Father affected

Type of father's malignancy
Beschrijving

Type of father's malignancy

Datatype

text

Sister affected
Beschrijving

Sister affected

Type of sister's malignancy
Beschrijving

Type of sister's malignancy

Datatype

text

Brother affected
Beschrijving

Brother affected

Type of brother's malignancy
Beschrijving

Type of brother's malignancy

Datatype

text

Hemato/Immunological diseases in the family
Beschrijving

Hemato/Immunological diseases in the family

Type of hemato-/immunological diseases
Beschrijving

Type of hemato-/immunological diseases

Datatype

text

Type of other diseases in the family
Beschrijving

Type of other diseases in the family

Type of other possibly relevant diseases
Beschrijving

Type of other possibly relevant diseases

Datatype

text

Similar models

Previous history

  1. StudyEvent: SE
    1. Previous history
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Dummy
Item
Dummy
text
Item
Xanthoma
integer
Code List
Xanthoma
CL Item
No (1)
CL Item
Yes (2)
Item
Café-au-lait spots
integer
Code List
Café-au-lait spots
CL Item
No (1)
CL Item
Yes (2)
Item
Other symptoms of NF1
integer
Code List
Other symptoms of NF1
CL Item
No (1)
CL Item
Yes (2)
Item
1° relatives with NF1
integer
Code List
1° relatives with NF1
CL Item
No (1)
CL Item
Yes (2)
Item
Previous congenital bone marrow failure disorder
integer
Code List
Previous congenital bone marrow failure disorder
CL Item
No (1)
CL Item
Yes (2)
Item
Previous acquired bone marrow failure disorder
integer
Code List
Previous acquired bone marrow failure disorder
CL Item
No (1)
CL Item
Yes (2)
Item
Previous malignancy
integer
Code List
Previous malignancy
CL Item
No (1)
CL Item
Yes (2)
Item
Previous chemo-radiotherapy (CT and/or RT)
integer
Code List
Previous chemo-radiotherapy (CT and/or RT)
CL Item
No (1)
CL Item
Yes (2)
Item
Mental retardation
integer
Code List
Mental retardation
CL Item
No (1)
CL Item
Yes (2)
Item
Birth weight < third percentile
integer
Code List
Birth weight < third percentile
CL Item
No (1)
CL Item
Yes (2)
Item
Height < third percentile (at diagnosis)
integer
Code List
Height < third percentile (at diagnosis)
CL Item
No (1)
CL Item
Yes (2)
Item
Weight < third percentile (at diagnosis)
integer
Code List
Weight < third percentile (at diagnosis)
CL Item
No (1)
CL Item
Yes (2)
Item
Head circumference < third percentile (at diagnosis)
integer
Code List
Head circumference < third percentile (at diagnosis)
CL Item
No (1)
CL Item
Yes (2)
Item
Clinical evidence of PNH
integer
Code List
Clinical evidence of PNH
CL Item
No (1)
CL Item
Yes (2)
Item
Hepatitis/Hepatopathy
integer
Code List
Hepatitis/Hepatopathy
CL Item
No (1)
CL Item
Yes (2)
Item
Patient is twin
integer
Code List
Patient is twin
CL Item
No (1)
CL Item
Yes (2)
Item
Congenital abnormalities
integer
Code List
Congenital abnormalities
CL Item
No (1)
CL Item
Yes (2)
Item
Other abnormalities
integer
Code List
Other abnormalities
CL Item
No (1)
CL Item
Yes (2)
Item Group
Number of cafe au lait spots
Item
Number of Café-au-lait spots
integer
Code List
Number of Café-au-lait spots
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
CL Item
8 (8)
CL Item
9 (9)
CL Item
> (10)
Item
Neurofibroma of any type
integer
Code List
Neurofibroma of any type
CL Item
No (1)
CL Item
Yes (2)
Item
Plexiform neurofibroma
integer
Code List
Plexiform neurofibroma
CL Item
No (1)
CL Item
Yes (2)
Item
Freckling in the axillary or inguinal regions
integer
Code List
Freckling in the axillary or inguinal regions
CL Item
No (1)
CL Item
Yes (2)
Item
Optic glioma
integer
Code List
Optic glioma
CL Item
No (1)
CL Item
Yes (2)
Item
>= 2 Lisch nodules of the iris
integer
Code List
>= 2 Lisch nodules of the iris
CL Item
No (1)
CL Item
Yes (2)
Item
Osseous lesions associated with NF1
integer
Code List
Osseous lesions associated with NF1
CL Item
No (1)
CL Item
Yes (2)
Item
Mother
integer
Code List
Mother
CL Item
No (1)
CL Item
Yes (2)
Item
Father
integer
Code List
Father
CL Item
No (1)
CL Item
Yes (2)
Item
Sister
integer
Code List
Sister
CL Item
No (1)
CL Item
Yes (2)
Item
Brother
integer
Code List
Brother
CL Item
No (1)
CL Item
Yes (2)
Item
Other relatives
integer
Code List
Other relatives
CL Item
No (1)
CL Item
Yes (2)
Item
Previous congenital bone marrow failure disorder
integer
Code List
Previous congenital bone marrow failure disorder
CL Item
Shwachman Diamond Syndrome (1)
CL Item
Severe congenital neutropenia (SCN) (2)
CL Item
Diamond Blackfan Anemia (DBA) (3)
CL Item
cong. sideroblastic anemia (4)
CL Item
Fanconi Anemia (5)
CL Item
Dyskeratosis congenita (6)
CL Item
Other (99)
Type
Item
Other type of congenital BMF
text
Date of previous aBMF
Item
Date of previous aBMF
date
Code List
Type of aBMF
CL Item
SAA (1)
CL Item
Other (99)
Previous acquired bone marrow failure disorder
Item
Other type of aBMF
text
Date of previous malignancy
Item
Date of previous malignancy
date
Item
Type of previous malignancy
integer
Code List
Type of previous malignancy
CL Item
ALL (1)
CL Item
AML (2)
CL Item
NHL (3)
CL Item
Ewing sarcoma (4)
CL Item
Medulloblastoma (5)
CL Item
Neuroblastoma (6)
CL Item
Other (99)
Other type of previous malignancy
Item
Other type of previous malignancy
text
Type of chemo therapy
Item
Type of chemo therapy
text
Type of radiotherapy
Item
Type of radiotherapy
text
Item Group
Type of cong. abnormalities
Type of congenital abnormalities
Item
Type of congenital abnormalities
text
Item Group
Type of other abnormalties
Type of other abnormalities
Item
Type of other abnormalities
text
Item Group
Item
Type of twin
integer
Code List
Type of twin
CL Item
Monozygotic (1)
CL Item
Dizygotic (2)
Item Group
Item
Parents are consanguineous
integer
Code List
Parents are consanguineous
CL Item
No (1)
CL Item
Yes (2)
Item
History of malignancies in family (1° relatives)
integer
Code List
History of malignancies in family (1° relatives)
CL Item
No (1)
CL Item
Yes (2)
Item
History of hemato-/immunological diseases
integer
Code List
History of hemato-/immunological diseases
CL Item
No (1)
CL Item
Yes (2)
Item
History of other possibly relevant diseases
integer
Code List
History of other possibly relevant diseases
CL Item
No (1)
CL Item
Yes (2)
Item
Mother
integer
Code List
Mother
CL Item
No (1)
CL Item
Yes (2)
Item
Father
integer
Code List
Father
CL Item
No (1)
CL Item
Yes (2)
Item
Sister
integer
Code List
Sister
CL Item
No (1)
CL Item
Yes (2)
Item
Brother
integer
Code List
Brother
CL Item
No (1)
CL Item
Yes (2)
Type of mother's malignancy
Item
Type of mother's malignancy
text
Type of father's malignancy
Item
Type of father's malignancy
text
Type of sister's malignancy
Item
Type of sister's malignancy
text
Type of brother's malignancy
Item
Type of brother's malignancy
text
Type of Hemato-/ Immunological diseases
Item
Type of hemato-/immunological diseases
text
Type of other possibly relevant diseases
Item
Type of other possibly relevant diseases
text

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