ID

36695

Descripción

Pancreatic Nutritional Program for Weight Loss in Overweight/Obese Patients With Stage I-III Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02432950

Link

https://clinicaltrials.gov/show/NCT02432950

Palabras clave

Versiones (1)
  1. 2/6/19 2/6/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

2 de junio de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Obesity NCT02432950

Inglés

Eligibility Obesity NCT02432950

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT02432950
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with early-stage breast cancer (stage i-iii)
Descripción

Early-Stage Breast Carcinoma TNM Breast tumor staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2986665
UMLS CUI [1,2]
C0474926
patients who have or have not undergone chemotherapy are both eligible; if the patient has undergone chemotherapy she must have completed adjuvant chemotherapy for >= 3 months and =< 5 years prior to study enrollment
Descripción

Chemotherapy | Chemotherapy Absent | Adjuvant Chemotherapy Completed

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0085533
UMLS CUI [3,2]
C0205197
postmenopausal women defined by either: natural menopause with at least one year since last menses, or chemotherapy-induced menopause with at least one year since last menses and follicle-stimulating hormone (fsh) and estradiol levels within the postmenopausal range
Descripción

Postmenopausal state | Natural menopause | Menopause Chemotherapy Induced | Follicle stimulating hormone level Postmenopausal state | Estradiol level Postmenopausal state

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
UMLS CUI [2]
C0856856
UMLS CUI [3,1]
C0025320
UMLS CUI [3,2]
C0392920
UMLS CUI [3,3]
C0205263
UMLS CUI [4,1]
C0428406
UMLS CUI [4,2]
C0232970
UMLS CUI [5,1]
C1443016
UMLS CUI [5,2]
C0232970
body mass index (bmi) of 25-33 kg/m^2
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
patients undergoing current adjuvant endocrine therapy are eligible
Descripción

Hormone Therapy Adjuvant

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C1522673
patients must be willing to adhere to the pnp intervention and the entire 6-month study
Descripción

Adherence Program Pancreatic Nutritional | Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1510802
UMLS CUI [1,2]
C3484370
UMLS CUI [1,3]
C0030274
UMLS CUI [1,4]
C1521739
UMLS CUI [2]
C0525058
all patients must have the ability and the willingness to sign a written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who are diabetic
Descripción

Diabetic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0241863
patients whose bmi falls outside the eligible range (< 25 kg/m^2 or > 33 kg/m^2)
Descripción

Body mass index Ineligible

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1305855
UMLS CUI [1,2]
C1512714
patients with stage iv breast cancer
Descripción

Breast Carcinoma TNM Breast tumor staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0474926
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Similar models

Eligibility Obesity NCT02432950

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT02432950
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Early-Stage Breast Carcinoma TNM Breast tumor staging
Item
patients with early-stage breast cancer (stage i-iii)
boolean
C2986665 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
Chemotherapy | Chemotherapy Absent | Adjuvant Chemotherapy Completed
Item
patients who have or have not undergone chemotherapy are both eligible; if the patient has undergone chemotherapy she must have completed adjuvant chemotherapy for >= 3 months and =< 5 years prior to study enrollment
boolean
C0392920 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0085533 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
Postmenopausal state | Natural menopause | Menopause Chemotherapy Induced | Follicle stimulating hormone level Postmenopausal state | Estradiol level Postmenopausal state
Item
postmenopausal women defined by either: natural menopause with at least one year since last menses, or chemotherapy-induced menopause with at least one year since last menses and follicle-stimulating hormone (fsh) and estradiol levels within the postmenopausal range
boolean
C0232970 (UMLS CUI [1])
C0856856 (UMLS CUI [2])
C0025320 (UMLS CUI [3,1])
C0392920 (UMLS CUI [3,2])
C0205263 (UMLS CUI [3,3])
C0428406 (UMLS CUI [4,1])
C0232970 (UMLS CUI [4,2])
C1443016 (UMLS CUI [5,1])
C0232970 (UMLS CUI [5,2])
Body mass index
Item
body mass index (bmi) of 25-33 kg/m^2
boolean
C1305855 (UMLS CUI [1])
Hormone Therapy Adjuvant
Item
patients undergoing current adjuvant endocrine therapy are eligible
boolean
C0279025 (UMLS CUI [1,1])
C1522673 (UMLS CUI [1,2])
Adherence Program Pancreatic Nutritional | Protocol Compliance
Item
patients must be willing to adhere to the pnp intervention and the entire 6-month study
boolean
C1510802 (UMLS CUI [1,1])
C3484370 (UMLS CUI [1,2])
C0030274 (UMLS CUI [1,3])
C1521739 (UMLS CUI [1,4])
C0525058 (UMLS CUI [2])
Informed Consent
Item
all patients must have the ability and the willingness to sign a written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetic
Item
patients who are diabetic
boolean
C0241863 (UMLS CUI [1])
Body mass index Ineligible
Item
patients whose bmi falls outside the eligible range (< 25 kg/m^2 or > 33 kg/m^2)
boolean
C1305855 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
Breast Carcinoma TNM Breast tumor staging
Item
patients with stage iv breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
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