ID

5312

Beskrivning

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/

Länk

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

Nyckelord

  1. 2014-08-05 2014-08-05 - Martin Dugas
  2. 2014-08-05 2014-08-05 - Martin Dugas
Uppladdad den

5 augusti 2014

DOI

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Licens

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
Beskrivning

Show identification of patient

Dummy
Beskrivning

Dummy

Datatyp

text

Previous history
Beskrivning

Previous history

Xanthoma
Beskrivning

Xanthoma

Datatyp

integer

Café-au-lait spots
Beskrivning

Café-au-lait spots

Datatyp

integer

Other symptoms of NF1
Beskrivning

Other symptoms of NF1

Datatyp

integer

1° relatives with NF1
Beskrivning

1° relatives with NF1

Datatyp

integer

Previous congenital bone marrow failure disorder
Beskrivning

Previous congenital bone marrow failure disorder

Datatyp

integer

Previous acquired bone marrow failure disorder
Beskrivning

Previous acquired bone marrow failure disorder

Datatyp

integer

Previous malignancy
Beskrivning

Previous malignancy

Datatyp

integer

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

Previous chemo-radiotherapy (CT and/or RT)

Datatyp

integer

Mental retardation
Beskrivning

Mental retardation

Datatyp

integer

Birth weight < third percentile
Beskrivning

Birth weight < third percentile

Datatyp

integer

Height < third percentile (at diagnosis)
Beskrivning

Height < third percentile (at diagnosis)

Datatyp

integer

Weight < third percentile (at diagnosis)
Beskrivning

Weight < third percentile (at diagnosis)

Datatyp

integer

Head circumference < third percentile (at diagnosis)
Beskrivning

Head circumference < third percentile (at diagnosis)

Datatyp

integer

Clinical evidence of PNH
Beskrivning

Clinical evidence of PNH

Datatyp

integer

Hepatitis/Hepatopathy
Beskrivning

Hepatitis/Hepatopathy

Datatyp

integer

Patient is twin
Beskrivning

Patient is twin

Datatyp

integer

Congenital abnormalities
Beskrivning

Congenital abnormalities

Datatyp

integer

Other abnormalities
Beskrivning

Other abnormalities

Datatyp

integer

Number of cafe au lait spots
Beskrivning

Number of cafe au lait spots

Number of Café-au-lait spots
Beskrivning

Number of Café-au-lait spots

Datatyp

integer

Type of other NF1 Symptoms
Beskrivning

Type of other NF1 Symptoms

Neurofibroma of any type
Beskrivning

Neurofibromas of any type

Datatyp

integer

Plexiform neurofibroma
Beskrivning

Plexiform neurofibroma

Datatyp

integer

Freckling in the axillary or inguinal regions
Beskrivning

Freckling in the axillary or inguinal regions

Datatyp

integer

Optic glioma
Beskrivning

Optic glioma

Datatyp

integer

>= 2 Lisch nodules of the iris
Beskrivning

>= 2 Lisch nodules of the iris

Datatyp

integer

Osseous lesions associated with NF1
Beskrivning

Osseous lesions associated with NF1

Datatyp

integer

Degree of relationship of NF1 relatives
Beskrivning

Degree of relationship of NF1 relatives

Mother
Beskrivning

Mother

Datatyp

integer

Father
Beskrivning

Father

Datatyp

integer

Sister
Beskrivning

Sister

Datatyp

integer

Brother
Beskrivning

Brother

Datatyp

integer

Other relatives
Beskrivning

Other relatives

Datatyp

integer

Type of previous cBMF
Beskrivning

Type of previous cBMF

Previous congenital bone marrow failure disorder
Beskrivning

Previous congenital bone marrow failure disorder

Datatyp

integer

Other type of congenital BMF
Beskrivning

Type

Datatyp

text

Date and type of acquired BMF
Beskrivning

Date and type of acquired BMF

Date of previous aBMF
Beskrivning

Date of previous aBMF

Datatyp

date

Type of aBMF
Beskrivning

Previous acquired bone marrow failure disorder

Datatyp

integer

Other type of aBMF
Beskrivning

Previous acquired bone marrow failure disorder

Datatyp

text

Date and type of previous malignancy
Beskrivning

Date and type of previous malignancy

Date of previous malignancy
Beskrivning

Date of previous malignancy

Datatyp

date

Type of previous malignancy
Beskrivning

Type of previous malignancy

Datatyp

integer

Other type of previous malignancy
Beskrivning

Other type of previous malignancy

Datatyp

text

Type of previous chemo therapy
Beskrivning

Type of previous chemo therapy

Type of chemo therapy
Beskrivning

Type of chemo therapy

Datatyp

text

Type of radiotherapy
Beskrivning

Type of radiotherapy

Datatyp

text

Type of cong. abnormalities
Beskrivning

Type of cong. abnormalities

Type of congenital abnormalities
Beskrivning

Type of congenital abnormalities

Datatyp

text

Type of other abnormalties
Beskrivning

Type of other abnormalties

Type of other abnormalities
Beskrivning

Type of other abnormalities

Datatyp

text

Type of twin
Beskrivning

Type of twin

Type of twin
Beskrivning

Type of twin

Datatyp

integer

Family history
Beskrivning

Family history

Parents are consanguineous
Beskrivning

Parents are consanguineous

Datatyp

integer

History of malignancies in family (1° relatives)
Beskrivning

History of malignancies in family (1° relatives)

Datatyp

integer

History of hemato-/immunological diseases
Beskrivning

History of hemato-/immunological diseases

Datatyp

integer

History of other possibly relevant diseases
Beskrivning

History of other possibly relevant diseases

Datatyp

integer

Family history of malignancies
Beskrivning

Family history of malignancies

Mother
Beskrivning

Mother

Datatyp

integer

Father
Beskrivning

Father

Datatyp

integer

Sister
Beskrivning

Sister

Datatyp

integer

Brother
Beskrivning

Brother

Datatyp

integer

Mother affected
Beskrivning

Mother affected

Type of mother's malignancy
Beskrivning

Type of mother's malignancy

Datatyp

text

Father affected
Beskrivning

Father affected

Type of father's malignancy
Beskrivning

Type of father's malignancy

Datatyp

text

Sister affected
Beskrivning

Sister affected

Type of sister's malignancy
Beskrivning

Type of sister's malignancy

Datatyp

text

Brother affected
Beskrivning

Brother affected

Type of brother's malignancy
Beskrivning

Type of brother's malignancy

Datatyp

text

Hemato/Immunological diseases in the family
Beskrivning

Hemato/Immunological diseases in the family

Type of hemato-/immunological diseases
Beskrivning

Type of hemato-/immunological diseases

Datatyp

text

Type of other diseases in the family
Beskrivning

Type of other diseases in the family

Type of other possibly relevant diseases
Beskrivning

Type of other possibly relevant diseases

Datatyp

text

Similar models

Previous history

  1. StudyEvent: SE
    1. Previous history
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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