ID

34158

Beschrijving

Evaluation of Effectiveness of Acupuncture on Quality of Life in Patients With Breast Cancer Receiving Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01727362

Link

https://clinicaltrials.gov/show/NCT01727362

Trefwoorden

  1. 14-01-19 14-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01727362

Eligibility Breast Cancer NCT01727362

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed breast cancer (invasive, intraductal, hormone-sensitive and not hormone-sensitive, only locoregional metastases)
Beschrijving

ID.1

Datatype

boolean

current chemotherapy at mammazentrum hamburg with regimen fec/doc or ec/doc
Beschrijving

ID.2

Datatype

boolean

willingness to receive acupuncture within the next 6 month if randomized in acupuncture group
Beschrijving

ID.3

Datatype

boolean

willingness to refrain from acupuncture within the next 6 month if randomized in control group
Beschrijving

ID.4

Datatype

boolean

informed consent
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
distant metastases
Beschrijving

ID.6

Datatype

boolean

blood coagulation disorder and/or current use of anticoagulants
Beschrijving

ID.7

Datatype

boolean

serious acute or chronic mental or physical disorders
Beschrijving

ID.8

Datatype

boolean

clinically relevant cardiac arrhythmia symptoms
Beschrijving

ID.9

Datatype

boolean

insufficient german language ability
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Breast Cancer NCT01727362

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosed breast cancer (invasive, intraductal, hormone-sensitive and not hormone-sensitive, only locoregional metastases)
boolean
ID.2
Item
current chemotherapy at mammazentrum hamburg with regimen fec/doc or ec/doc
boolean
ID.3
Item
willingness to receive acupuncture within the next 6 month if randomized in acupuncture group
boolean
ID.4
Item
willingness to refrain from acupuncture within the next 6 month if randomized in control group
boolean
ID.5
Item
informed consent
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
distant metastases
boolean
ID.7
Item
blood coagulation disorder and/or current use of anticoagulants
boolean
ID.8
Item
serious acute or chronic mental or physical disorders
boolean
ID.9
Item
clinically relevant cardiac arrhythmia symptoms
boolean
ID.10
Item
insufficient german language ability
boolean

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