ID

12921

Description

Gene Therapy Plus Chemotherapy in Treating Patients With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00004038

Lien

https://clinicaltrials.gov/show/NCT00004038

Mots-clés

  1. 06/01/2016 06/01/2016 -
Détendeur de droits

CC BY-NC 3.0

Téléchargé le

6 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT00004038

Eligibility Breast Cancer NCT00004038

Criteria
Description

Criteria

histologically confirmed epithelial breast cancer
Description

breast cancer

Type de données

boolean

Alias
UMLS CUI [1]
C0678222
at least 3 cutaneous or subcutaneous lesions required
Description

cutaneous or subcutaneous lesions

Type de données

boolean

Alias
UMLS CUI [1]
C0221198
measurable disease that includes, but is not limited to, cutaneous or subcutaneous metastases
Description

measurable disease

Type de données

boolean

Alias
UMLS CUI [1]
C1513041
patient characteristics:
Description

patient characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
age: over 18
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
performance status: ecog 0-2
Description

performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
absolute granulocyte count at least 1,500/mm3
Description

absolute granulocyte count

Type de données

boolean

Alias
UMLS CUI [1]
C0857490
hemoglobin greater than 8 g/dl
Description

hemoglobin

Type de données

boolean

Alias
UMLS CUI [1]
C0019046
platelet count greater than 100,000/mm3
Description

platelet count

Type de données

boolean

Alias
UMLS CUI [1]
C0005821
bilirubin less than 2 mg/dl
Description

bilirubin

Type de données

boolean

Alias
UMLS CUI [1]
C1278039
pt/ptt within normal range
Description

pt/ptt

Type de données

boolean

Alias
UMLS CUI [1]
C0030605
sgot/sgpt less than 2 times upper limit of normal
Description

sgot/sgpt

Type de données

boolean

Alias
UMLS CUI [1]
C0201836
UMLS CUI [2]
C0201899
creatinine less than 1.8 mg/dl
Description

creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
not pregnant
Description

pregnant

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
fertile patients must use effective contraception during and for 3 months after therapy
Description

contraception

Type de données

boolean

Alias
UMLS CUI [1]
C0700589
prior concurrent therapy:
Description

prior concurrent therapy:

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
concurrent cytotoxic chemotherapy allowed, if stable and responding
Description

chemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
at least 4 weeks since prior chemotherapy, if starting a new regimen
Description

at least 4 weeks since prior chemotherapy, if starting a new regimen

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
at least 4 weeks since radiotherapy
Description

radiotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C1522449
prior adjuvant radiotherapy to the chest wall allowed
Description

prior adjuvant radiotherapy to the chest wall allowed

Type de données

boolean

Alias
UMLS CUI [1]
C1522449
at least 6 months since radiotherapy to lesions that are to be injected
Description

at least 6 months since radiotherapy to lesions that are to be injected

Type de données

boolean

Alias
UMLS CUI [1]
C1522449
recovered from prior therapy
Description

recovered from prior therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0087111

Similar models

Eligibility Breast Cancer NCT00004038

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
breast cancer
Item
histologically confirmed epithelial breast cancer
boolean
C0678222 (UMLS CUI [1])
cutaneous or subcutaneous lesions
Item
at least 3 cutaneous or subcutaneous lesions required
boolean
C0221198 (UMLS CUI [1])
measurable disease
Item
measurable disease that includes, but is not limited to, cutaneous or subcutaneous metastases
boolean
C1513041 (UMLS CUI [1])
patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
age
Item
age: over 18
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status: ecog 0-2
boolean
C1520224 (UMLS CUI [1])
absolute granulocyte count
Item
absolute granulocyte count at least 1,500/mm3
boolean
C0857490 (UMLS CUI [1])
hemoglobin
Item
hemoglobin greater than 8 g/dl
boolean
C0019046 (UMLS CUI [1])
platelet count
Item
platelet count greater than 100,000/mm3
boolean
C0005821 (UMLS CUI [1])
bilirubin
Item
bilirubin less than 2 mg/dl
boolean
C1278039 (UMLS CUI [1])
pt/ptt
Item
pt/ptt within normal range
boolean
C0030605 (UMLS CUI [1])
sgot/sgpt
Item
sgot/sgpt less than 2 times upper limit of normal
boolean
C0201836 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
creatinine
Item
creatinine less than 1.8 mg/dl
boolean
C0201976 (UMLS CUI [1])
pregnant
Item
not pregnant
boolean
C0032961 (UMLS CUI [1])
contraception
Item
fertile patients must use effective contraception during and for 3 months after therapy
boolean
C0700589 (UMLS CUI [1])
prior concurrent therapy:
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
chemotherapy
Item
concurrent cytotoxic chemotherapy allowed, if stable and responding
boolean
C0392920 (UMLS CUI [1])
at least 4 weeks since prior chemotherapy, if starting a new regimen
Item
at least 4 weeks since prior chemotherapy, if starting a new regimen
boolean
C0392920 (UMLS CUI [1])
radiotherapy
Item
at least 4 weeks since radiotherapy
boolean
C1522449 (UMLS CUI [1])
prior adjuvant radiotherapy to the chest wall allowed
Item
prior adjuvant radiotherapy to the chest wall allowed
boolean
C1522449 (UMLS CUI [1])
at least 6 months since radiotherapy to lesions that are to be injected
Item
at least 6 months since radiotherapy to lesions that are to be injected
boolean
C1522449 (UMLS CUI [1])
recovered from prior therapy
Item
recovered from prior therapy
boolean
C0087111 (UMLS CUI [1])

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