ID

42032

Beskrivning

International Collaborative Treatment Protocol For Children And Adolescents With Acute Lymphoblastic Leukemia. Phase 3 Study. Registry Formular (Please send this to study centre until Day 8) Clinical Trial Number: NCT01117441.

Nyckelord

  1. 2016-05-21 2016-05-21 -
  2. 2021-03-15 2021-03-15 - Dr. rer. medic Philipp Neuhaus
Uppladdad den

15 mars 2021

DOI

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Creative Commons BY-NC-ND 3.0

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Registry Formular AIEOP-BFM ALL 2009 DRKS00003772 NCT01117441

Registry Formular AIEOP-BFM ALL 2009 NCT01117441

Patient Information
Beskrivning

Patient Information

Alias
UMLS CUI-1
C1955348
Patient name
Beskrivning

Patient name

Datatyp

text

Alias
UMLS CUI [1]
C1299487
Patient Birth Date
Beskrivning

Patient Birth Date

Datatyp

date

Alias
UMLS CUI [1]
C0421451
Patient's gender
Beskrivning

Gender

Datatyp

text

Alias
UMLS CUI [1]
C0079399
Date of diagnosis
Beskrivning

Date of diagnosis

Datatyp

date

Alias
UMLS CUI [1]
C2316983
Therapy start date (start of pre-phase)
Beskrivning

Therapy start date

Datatyp

date

Alias
UMLS CUI [1]
C3173309
Eligibility Criteria
Beskrivning

Eligibility Criteria

Alias
UMLS CUI-1
C0013893
Diagnosis of primary ALL
Beskrivning

Diagnosis of primary ALL

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0023449
UMLS CUI [1,2]
C0011900
Exclusion of BCR/ABL-rearrangement or translocation t(9;22)?
Beskrivning

BCR/ABL-rearrangement or t(9;22)

Datatyp

boolean

Alias
UMLS CUI [1]
C0004891
UMLS CUI [2]
C3897138
Exclusion of pregnancy or nursing?
Beskrivning

Pregnancy or nursing

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
Does patient participate in another study trial? (Except for associated studies)
Beskrivning

Study Participation status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
Informed consent given by person who has custody of child (if patient > 15 y/o, informed consent given by patient himself/ herself) to participate in study and data storage
Beskrivning

Informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Did patient receive steroids (longer than 2 weeks; dosage >= 1 mg/kg/d) or cytostatics 4 weeks before diagnosis?
Beskrivning

Steroid therapy and chemotherapy regimen

Datatyp

boolean

Alias
UMLS CUI [1]
C0149783
UMLS CUI [2]
C0392920
Does the patient has any comorbidity which is interferring with study protocol?
Beskrivning

Comorbidity affecting study protocol

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C2348563
If Patient received steroid therapy (longer than 2 weeks; dosage >= 1 mg/kg/d) or cytostatics 4 weeks before diagnosis, specify:
Beskrivning

If Patient received steroid therapy (longer than 2 weeks; dosage >= 1 mg/kg/d) or cytostatics 4 weeks before diagnosis, specify:

Alias
UMLS CUI-1
C0149783
UMLS CUI-2
C0392920
Specify steroid therapy and chemotherapy regimen:
Beskrivning

Steroid therapy and chemotherapy regimen: Specification

Datatyp

text

Alias
UMLS CUI [1,1]
C0149783
UMLS CUI [1,2]
C2348235
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C2348235
Specify received daily dose:
Beskrivning

Daily Dose

Datatyp

float

Alias
UMLS CUI [1]
C2348070
Specify start date of therapy:
Beskrivning

Start date

Datatyp

date

Alias
UMLS CUI [1]
C0808070
Specify last date of therapy:
Beskrivning

End date

Datatyp

date

Alias
UMLS CUI [1]
C0806020
Informed consent to participate in Concomitant studies and for storage of clinical samples
Beskrivning

Informed consent to participate in Concomitant studies and for storage of clinical samples

Alias
UMLS CUI-1
C0021430
UMLS CUI-2
C0521115
UMLS CUI-3
C0008976
UMLS CUI-5
C0021430
UMLS CUI-6
C3242025
Early diagnosis of high risk patient for relapse?
Beskrivning

High risk for relapse

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0684030
UMLS CUI [1,2]
C0277556
Moleculargenetic evidence of minimal CNS leukemia?
Beskrivning

CNS leukemia

Datatyp

boolean

Alias
UMLS CUI [1]
C1332884
Diagnostic meaning of IL-15 in CNS-leukemia?
Beskrivning

IL-15 and CNS leukemia

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0254610
UMLS CUI [1,2]
C1332884
Genetic change in leukemic cells and its prognostic meaning?
Beskrivning

Genetic change in leukemic cells

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1517806
UMLS CUI [1,2]
C1705285
Genetic variation as risk factors for severe infections (during chemotherapy)?
Beskrivning

Genetic variation as risk factors for infections

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1705285
UMLS CUI [1,2]
C0035648
UMLS CUI [1,3]
C0009450
Storage of clinical samples for future trials about leukemia?
Beskrivning

Storage of clinical samples: Leukemia trials

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3242025
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0023418
Storage of clinical samples for future trials about host cells -target?
Beskrivning

Storage of clinical samples: host cells -target- trials

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3242025
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1819995
UMLS CUI [1,4]
C1521840
Storage of clinical samples for future trials about host cells -whole genom?
Beskrivning

Storage of clinical samples: host cells -whole genom- trials

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3242025
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1819995
UMLS CUI [1,4]
C2350277
Laboratory Diagnostic
Beskrivning

Laboratory Diagnostic

Alias
UMLS CUI-1
C1254361
Immunologic tests
Beskrivning

Immunologic tests

Datatyp

text

Alias
UMLS CUI [1]
C0021061
If immunologic tests were performed in not-referrence laboratory, specify:
Beskrivning

Immunologic tests: Specification

Datatyp

text

Alias
UMLS CUI [1,1]
C0021061
UMLS CUI [1,2]
C2348235
Karyotypization and Moleculargenetics (RT-PCR, FISH for diagnosis of TEL/AML1, BCR/ABL, MLL-Rearrangements, others)
Beskrivning

Karyotypization and Moleculargenetics

Datatyp

text

Alias
UMLS CUI [1]
C0022526
UMLS CUI [2]
C1948182
If Karyotypization and Moleculargenetics were performed, specify laboratory:
Beskrivning

Karyotypization and Moleculargenetics: Specification

Datatyp

text

Alias
UMLS CUI [1,1]
C0022526
UMLS CUI [1,2]
C2348235
UMLS CUI [2,1]
C1948182
UMLS CUI [2,2]
C2348235
Identification and Signature
Beskrivning

Identification and Signature

Alias
UMLS CUI-1
C0205396
UMLS CUI-2
C1519316
Doctor's Name
Beskrivning

Doctor's Name

Datatyp

text

Alias
UMLS CUI [1,1]
C0027365
UMLS CUI [1,2]
C0031831
Date of report
Beskrivning

Date of report

Datatyp

date

Alias
UMLS CUI [1]
C1302584
Doctor's signature
Beskrivning

Signature

Datatyp

text

Alias
UMLS CUI [1]
C1519316

Similar models

Registry Formular AIEOP-BFM ALL 2009 NCT01117441

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Patient Information
C1955348 (UMLS CUI-1)
Patient name
Item
Patient name
text
C1299487 (UMLS CUI [1])
Patient Birth Date
Item
Patient Birth Date
date
C0421451 (UMLS CUI [1])
Item
Patient's gender
text
C0079399 (UMLS CUI [1])
Code List
Patient's gender
CL Item
Male (Male)
CL Item
Female (Female)
Date of diagnosis
Item
Date of diagnosis
date
C2316983 (UMLS CUI [1])
Therapy start date
Item
Therapy start date (start of pre-phase)
date
C3173309 (UMLS CUI [1])
Item Group
Eligibility Criteria
C0013893 (UMLS CUI-1)
Diagnosis of primary ALL
Item
Diagnosis of primary ALL
boolean
C0023449 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
BCR/ABL-rearrangement or t(9;22)
Item
Exclusion of BCR/ABL-rearrangement or translocation t(9;22)?
boolean
C0004891 (UMLS CUI [1])
C3897138 (UMLS CUI [2])
Pregnancy or nursing
Item
Exclusion of pregnancy or nursing?
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Participation status
Item
Does patient participate in another study trial? (Except for associated studies)
boolean
C2348568 (UMLS CUI [1])
Informed consent
Item
Informed consent given by person who has custody of child (if patient > 15 y/o, informed consent given by patient himself/ herself) to participate in study and data storage
boolean
C0021430 (UMLS CUI [1])
Steroid therapy and chemotherapy regimen
Item
Did patient receive steroids (longer than 2 weeks; dosage >= 1 mg/kg/d) or cytostatics 4 weeks before diagnosis?
boolean
C0149783 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
Comorbidity affecting study protocol
Item
Does the patient has any comorbidity which is interferring with study protocol?
boolean
C0009488 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
Item Group
If Patient received steroid therapy (longer than 2 weeks; dosage >= 1 mg/kg/d) or cytostatics 4 weeks before diagnosis, specify:
C0149783 (UMLS CUI-1)
C0392920 (UMLS CUI-2)
Steroid therapy and chemotherapy regimen: Specification
Item
Specify steroid therapy and chemotherapy regimen:
text
C0149783 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
Daily Dose
Item
Specify received daily dose:
float
C2348070 (UMLS CUI [1])
Start date
Item
Specify start date of therapy:
date
C0808070 (UMLS CUI [1])
End date
Item
Specify last date of therapy:
date
C0806020 (UMLS CUI [1])
Item Group
Informed consent to participate in Concomitant studies and for storage of clinical samples
C0021430 (UMLS CUI-1)
C0521115 (UMLS CUI-2)
C0008976 (UMLS CUI-3)
C0021430 (UMLS CUI-5)
C3242025 (UMLS CUI-6)
High risk for relapse
Item
Early diagnosis of high risk patient for relapse?
boolean
C0684030 (UMLS CUI [1,1])
C0277556 (UMLS CUI [1,2])
CNS leukemia
Item
Moleculargenetic evidence of minimal CNS leukemia?
boolean
C1332884 (UMLS CUI [1])
IL-15 and CNS leukemia
Item
Diagnostic meaning of IL-15 in CNS-leukemia?
boolean
C0254610 (UMLS CUI [1,1])
C1332884 (UMLS CUI [1,2])
Genetic change in leukemic cells
Item
Genetic change in leukemic cells and its prognostic meaning?
boolean
C1517806 (UMLS CUI [1,1])
C1705285 (UMLS CUI [1,2])
Genetic variation as risk factors for infections
Item
Genetic variation as risk factors for severe infections (during chemotherapy)?
boolean
C1705285 (UMLS CUI [1,1])
C0035648 (UMLS CUI [1,2])
C0009450 (UMLS CUI [1,3])
Storage of clinical samples: Leukemia trials
Item
Storage of clinical samples for future trials about leukemia?
boolean
C3242025 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0023418 (UMLS CUI [1,3])
Storage of clinical samples: host cells -target- trials
Item
Storage of clinical samples for future trials about host cells -target?
boolean
C3242025 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1819995 (UMLS CUI [1,3])
C1521840 (UMLS CUI [1,4])
Storage of clinical samples: host cells -whole genom- trials
Item
Storage of clinical samples for future trials about host cells -whole genom?
boolean
C3242025 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1819995 (UMLS CUI [1,3])
C2350277 (UMLS CUI [1,4])
Item Group
Laboratory Diagnostic
C1254361 (UMLS CUI-1)
Item
Immunologic tests
text
C0021061 (UMLS CUI [1])
Code List
Immunologic tests
CL Item
Not performed (Not performed)
CL Item
Performed: in referrence laboratory (Berlin-Buch, Prof. Ludwig) (Performed: in referrence laboratory (Berlin-Buch, Prof. Ludwig))
CL Item
Performed: not in referrence laboratory (Performed: not in referrence laboratory)
Immunologic tests: Specification
Item
If immunologic tests were performed in not-referrence laboratory, specify:
text
C0021061 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
Karyotypization and Moleculargenetics (RT-PCR, FISH for diagnosis of TEL/AML1, BCR/ABL, MLL-Rearrangements, others)
text
C0022526 (UMLS CUI [1])
C1948182 (UMLS CUI [2])
Code List
Karyotypization and Moleculargenetics (RT-PCR, FISH for diagnosis of TEL/AML1, BCR/ABL, MLL-Rearrangements, others)
CL Item
Not performed (Not performed)
CL Item
Performed: in referrence laboratory (Performed: in referrence laboratory )
CL Item
Performed: not in referrence laboratory (Performed: not in referrence laboratory)
Karyotypization and Moleculargenetics: Specification
Item
If Karyotypization and Moleculargenetics were performed, specify laboratory:
text
C0022526 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
C1948182 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
Item Group
Identification and Signature
C0205396 (UMLS CUI-1)
C1519316 (UMLS CUI-2)
Doctor's Name
Item
Doctor's Name
text
C0027365 (UMLS CUI [1,1])
C0031831 (UMLS CUI [1,2])
Date of report
Item
Date of report
date
C1302584 (UMLS CUI [1])
Signature
Item
Doctor's signature
text
C1519316 (UMLS CUI [1])

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