ID

16304

Beschrijving

Placebo-controlled Evaluation of Cocculine® Efficacy in the Management of Nausea After Chemotherapy in Breast Cancer.; ODM derived from: https://clinicaltrials.gov/show/NCT00409071

Link

https://clinicaltrials.gov/show/NCT00409071

Trefwoorden

  1. 10-07-16 10-07-16 -
Geüploaded op

10 juli 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00409071

Eligibility Breast Cancer NCT00409071

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
women with histologically proven non metastatic breast cancer
Beschrijving

women with non metastatic breast cancer

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0678222
UMLS CUI [1,3]
C1300072
no previous chemotherapy
Beschrijving

Previous chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1514457
treatment planning including 6 adjuvant ct courses with the first 3 being necessarily of the fac50, fec100 or tac type
Beschrijving

treatment planning including 6 adjuvant ct courses

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085533
UMLS CUI [1,2]
C1301732
age>= 18 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance status (ps) <= 2 (who scale)
Beschrijving

ECOG

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
patient able to read and understand french
Beschrijving

language

Datatype

boolean

Alias
UMLS CUI [1]
C1145677
written, voluntary, informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous treatment with chemotherapy (including neo-adjuvant chemotherapy for breast cancer)
Beschrijving

previous treatment with chemotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0678222
previous malignancies (except basal cell skin cancer or cervical cancer in situ or any other curatively treated malignancy in complete remission for more than 5 years)
Beschrijving

previous malignancies

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
contraindication to corticosteroids or 5-ht3 receptor antagonists
Beschrijving

contraindication to corticosteroids or 5-ht3 receptor antagonists

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0001617
UMLS CUI [1,3]
C2936526
treatment with cocculine® or any other anti-emetic drug in the 15 days before inclusion
Beschrijving

treatment with anti-emetic drugs

Datatype

boolean

Alias
UMLS CUI [1]
C0003297
pregnant or lactating women
Beschrijving

pregnant or lactating women

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
follow-up impossible for social, geographical, familial or psychological reasons
Beschrijving

follow-up

Datatype

boolean

Alias
UMLS CUI [1]
C1522577
patients who cannot be contacted by phone
Beschrijving

Telephone

Datatype

boolean

Alias
UMLS CUI [1]
C0039457

Similar models

Eligibility Breast Cancer NCT00409071

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
women with non metastatic breast cancer
Item
women with histologically proven non metastatic breast cancer
boolean
C0079399 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C1300072 (UMLS CUI [1,3])
Previous chemotherapy
Item
no previous chemotherapy
boolean
C1514457 (UMLS CUI [1])
treatment planning including 6 adjuvant ct courses
Item
treatment planning including 6 adjuvant ct courses with the first 3 being necessarily of the fac50, fec100 or tac type
boolean
C0085533 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
age
Item
age>= 18 years
boolean
C0001779 (UMLS CUI [1])
ECOG
Item
ecog performance status (ps) <= 2 (who scale)
boolean
C1520224 (UMLS CUI [1])
language
Item
patient able to read and understand french
boolean
C1145677 (UMLS CUI [1])
Informed Consent
Item
written, voluntary, informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
previous treatment with chemotherapy
Item
previous treatment with chemotherapy (including neo-adjuvant chemotherapy for breast cancer)
boolean
C1514457 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
previous malignancies
Item
previous malignancies (except basal cell skin cancer or cervical cancer in situ or any other curatively treated malignancy in complete remission for more than 5 years)
boolean
C0006826 (UMLS CUI [1])
contraindication to corticosteroids or 5-ht3 receptor antagonists
Item
contraindication to corticosteroids or 5-ht3 receptor antagonists
boolean
C1301624 (UMLS CUI [1,1])
C0001617 (UMLS CUI [1,2])
C2936526 (UMLS CUI [1,3])
treatment with anti-emetic drugs
Item
treatment with cocculine® or any other anti-emetic drug in the 15 days before inclusion
boolean
C0003297 (UMLS CUI [1])
pregnant or lactating women
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
follow-up
Item
follow-up impossible for social, geographical, familial or psychological reasons
boolean
C1522577 (UMLS CUI [1])
Telephone
Item
patients who cannot be contacted by phone
boolean
C0039457 (UMLS CUI [1])

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