ID
12426
Description
Hyper-PEI-protocol:a programme with regional deep hyperthermia(RHT)in combination with PEI-chemotherapy.The Hyper-PEI protocol is offered in place of the intensive standard chemotherapy for high-risk patie nts with malignant, extracranial tumors. Patients have a measurable relapsed tumor,or a primary tumor that did not respond sufficiently to treatment according to standard protocols. Responsible MD: PD Dr. med. R Wessalowski, Clinic for pediatric oncology,haematology and immunology UKD, Moorenstr. 5, 40225 Dusseldorf Form has to be completed by cooperating center or clinic and sent to the Hyper-PEI director. Confirmation or denial of admittance will be sent to the cooperating center and GPOH study coordinator by head of protocol.
Keywords
Versions (2)
- 11/17/15 11/17/15 - Julian Varghese
- 11/17/15 11/17/15 - Julian Varghese
Uploaded on
November 17, 2015
DOI
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License
Creative Commons BY-NC 3.0
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Admission and Eligiblity Form Hyperthermia Treatment Study
Admission and Eligibility
- StudyEvent: ODM
Description
Date
Alias
- UMLS CUI-1
- C0011008
Description
Inclusion criteria
Alias
- UMLS CUI-1
- C1512693
Description
Histologically significant solid tumor
Data type
boolean
Alias
- UMLS CUI [1]
- C1698088
Description
no metastases
Data type
boolean
Alias
- UMLS CUI [1]
- C0445092
Description
Only if prognosis of patient can be improved significantly through treatment of tumor-section
Data type
boolean
Alias
- UMLS CUI [1]
- C0027627
Description
Staging
Data type
boolean
Alias
- UMLS CUI [1]
- C1515169
Description
Other study
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
Description
age
Data type
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
Informed consent
Data type
boolean
Alias
- UMLS CUI [1]
- C0021430
Description
Lansky/Karnovsky score
Data type
boolean
Alias
- UMLS CUI [1]
- C1522275
Description
Life expectancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0023671
Description
Blood count
Data type
boolean
Alias
- UMLS CUI [1]
- C0005771
Description
Platelets
Data type
boolean
Alias
- UMLS CUI [1]
- C1287267
Description
Creatinine
Data type
boolean
Alias
- UMLS CUI [1]
- C0201976
Description
Creatinine clearance
Data type
boolean
Alias
- UMLS CUI [1]
- C0373595
Description
Transaminases
Data type
boolean
Alias
- UMLS CUI [1]
- C0002594
Description
Bilirubin
Data type
boolean
Alias
- UMLS CUI [1]
- C1278039
Description
Coagulation
Data type
boolean
Alias
- UMLS CUI [1]
- C0005778
Description
Leukapheresis
Data type
boolean
Alias
- UMLS CUI [1]
- C0023416
- UMLS CUI [2]
- C0398523
Description
Comments
Data type
text
Alias
- UMLS CUI [1]
- C0947611
Description
Exclusion criteria
Alias
- UMLS CUI-1
- C0680251
Description
Pacemaker
Data type
boolean
Alias
- UMLS CUI [1]
- C0030163
Description
if need be consult with study coordinator
Data type
boolean
Alias
- UMLS CUI [1]
- C0021102
Description
Metastasis
Data type
boolean
Alias
- UMLS CUI [1]
- C0027627
Description
Pregnancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Hepatitis B
Data type
boolean
Alias
- UMLS CUI [1]
- C0019196
- UMLS CUI [2]
- C0019163
Description
HIV
Data type
boolean
Alias
- UMLS CUI [1]
- C0019699
Description
Comment
Data type
text
Alias
- UMLS CUI [1]
- C0947611
Description
Attachment
Alias
- UMLS CUI-1
- C1999228
Description
Correctness of information confirmed
Alias
- UMLS CUI-1
- C0521091
- UMLS CUI-2
- C1533716
Description
Inclusion of Patient into Hyper-PEI Protocol
Alias
- UMLS CUI-1
- C1512693
Similar models
Admission and Eligibility
- StudyEvent: ODM
C0398523 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C0019163 (UMLS CUI [2])
C1533716 (UMLS CUI-2)