Information:
Error:
ID
13139
Description
Effect of Oral Supplementation With a Fibre Enriched Paediatric Sip Feed For Children With Acute Lymphocytic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT01600781
Link
https://clinicaltrials.gov/show/NCT01600781
Keywords
Versions (1)
- 1/19/16 1/19/16 -
Copyright Holder
CC BY-NC 3.0
Uploaded on
January 19, 2016
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Acute Lymphocytic Leukemia NCT01600781
Eligibility Acute Lymphocytic Leukemia NCT01600781
- StudyEvent: Eligibility
Similar models
Eligibility Acute Lymphocytic Leukemia NCT01600781
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
age
Item
age should be above 2 years and children should be pre-pubertal.
boolean
C0001779 (UMLS CUI [1])
hospitalization
Item
hospitalized for the entire (6 week) intervention period.
boolean
C0019993 (UMLS CUI [1])
chemotherapy
Item
about to receive? induction chemotherapy.
boolean
C0392920 (UMLS CUI [1])
oral feeding
Item
able to tolerate oral feeding.
boolean
C0349717 (UMLS CUI [1])
informed consent
Item
written informed consent from parents/guardian (and child, if applicable to local law).
boolean
C0021430 (UMLS CUI [1])
all patients < 2 years and those who show signs of puberty
Item
all patients < 2 years and those who show signs of puberty.
boolean
C0001779 (UMLS CUI [1])
all patients who cannot tolerate oral feeding and/or are on parenteral nutrition
Item
all patients who cannot tolerate oral feeding and/or are on parenteral nutrition.
boolean
C0349717 (UMLS CUI [1])
C0030547 (UMLS CUI [2])
C0030547 (UMLS CUI [2])
cow's milk allergy/intolerance or galactosemia
Item
all patients with a known history of cow's milk allergy/intolerance or galactosemia.
boolean
C0020517 (UMLS CUI [1,1])
C0349374 (UMLS CUI [1,2])
C0016952 (UMLS CUI [2])
C0349374 (UMLS CUI [1,2])
C0016952 (UMLS CUI [2])
diet
Item
all patients requiring a fibre-free diet.
boolean
C0012155 (UMLS CUI [1])
investigator's uncertainty about the willingness or ability of the child/carer to comply with the protocol requirements
Item
investigator's uncertainty about the willingness or ability of the child/carer to comply with the protocol requirements.
boolean
C1321605 (UMLS CUI [1])
participation in any other study involving investigational or marketed products concomitantly or within two weeks prior to entry into the study
Item
participation in any other study involving investigational or marketed products concomitantly or within two weeks prior to entry into the study.
boolean
C2348568 (UMLS CUI [1])