ID

23643

Descripción

Chronic Pain in Women Who Have Undergone Surgery for Stage I, Stage II, or Stage III Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00971919

Link

https://clinicaltrials.gov/show/NCT00971919

Palabras clave

  1. 10/7/17 10/7/17 -
Subido en

10 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00971919

Eligibility Breast Cancer NCT00971919

Criteria
Descripción

Criteria

histologically confirmed invasive breast cancer or carcinoma in situ of the breast by core biopsy or fine needle aspiration
Descripción

Invasive carcinoma of breast | Carcinoma in situ of female breast | Core needle biopsy | Fine needle aspiration

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0853879
UMLS CUI [2]
C0686288
UMLS CUI [3]
C1318309
UMLS CUI [4]
C1510483
newly diagnosed disease
Descripción

Newly Diagnosed Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1334965
stage i-iii disease
Descripción

Disease TNM Breast tumor staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0474926
resectable disease
Descripción

Disease Resectable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1514888
being treated in the aberdeen, dundee, perth, or inverness breast unit
Descripción

Therapeutic procedure Breast clinic Specified

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C3810844
UMLS CUI [1,3]
C0205369
planning to undergo primary surgical excision of the tumor (e.g., breast conservation surgery or mastectomy with or without axillary surgery [sentinel node biopsy, axillary sample, or axillary clearance])
Descripción

Excision of neoplasm Primary Planned | Breast-Conserving Surgery | Mastectomy | Operative Surgical Procedures Axillary | Sentinel Lymph Node Biopsy | Sample Axillary | Axillary clearance

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1299802
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C1301732
UMLS CUI [2]
C0917927
UMLS CUI [3]
C0024881
UMLS CUI [4,1]
C0543467
UMLS CUI [4,2]
C0004454
UMLS CUI [5]
C0796693
UMLS CUI [6,1]
C0370003
UMLS CUI [6,2]
C0004454
UMLS CUI [7]
C4087394
planning to undergo standard adjuvant therapy after surgery, including radiotherapy, chemotherapy, and/or hormonal therapy, as per existing standard protocols
Descripción

Adjuvant therapy Standard Postoperative Planned | Therapeutic radiology procedure | Chemotherapy | Hormone Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0677850
UMLS CUI [1,2]
C1442989
UMLS CUI [1,3]
C0032790
UMLS CUI [1,4]
C1301732
UMLS CUI [2]
C1522449
UMLS CUI [3]
C0392920
UMLS CUI [4]
C0279025
no detectable metastatic disease
Descripción

Neoplasm Metastasis Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0332197
patient characteristics:
Descripción

Client Characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
not pregnant
Descripción

Pregnancy Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
speaks english
Descripción

Able to speak English Language

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
no history of mental illness
Descripción

Mental disorders Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0332197
prior concurrent therapy:
Descripción

Prior Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514463
see disease characteristics
Descripción

ID.14

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer NCT00971919

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Invasive carcinoma of breast | Carcinoma in situ of female breast | Core needle biopsy | Fine needle aspiration
Item
histologically confirmed invasive breast cancer or carcinoma in situ of the breast by core biopsy or fine needle aspiration
boolean
C0853879 (UMLS CUI [1])
C0686288 (UMLS CUI [2])
C1318309 (UMLS CUI [3])
C1510483 (UMLS CUI [4])
Newly Diagnosed Disease
Item
newly diagnosed disease
boolean
C1334965 (UMLS CUI [1])
Disease TNM Breast tumor staging
Item
stage i-iii disease
boolean
C0012634 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
Disease Resectable
Item
resectable disease
boolean
C0012634 (UMLS CUI [1,1])
C1514888 (UMLS CUI [1,2])
Therapeutic procedure Breast clinic Specified
Item
being treated in the aberdeen, dundee, perth, or inverness breast unit
boolean
C0087111 (UMLS CUI [1,1])
C3810844 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Excision of neoplasm Primary Planned | Breast-Conserving Surgery | Mastectomy | Operative Surgical Procedures Axillary | Sentinel Lymph Node Biopsy | Sample Axillary | Axillary clearance
Item
planning to undergo primary surgical excision of the tumor (e.g., breast conservation surgery or mastectomy with or without axillary surgery [sentinel node biopsy, axillary sample, or axillary clearance])
boolean
C1299802 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0917927 (UMLS CUI [2])
C0024881 (UMLS CUI [3])
C0543467 (UMLS CUI [4,1])
C0004454 (UMLS CUI [4,2])
C0796693 (UMLS CUI [5])
C0370003 (UMLS CUI [6,1])
C0004454 (UMLS CUI [6,2])
C4087394 (UMLS CUI [7])
Adjuvant therapy Standard Postoperative Planned | Therapeutic radiology procedure | Chemotherapy | Hormone Therapy
Item
planning to undergo standard adjuvant therapy after surgery, including radiotherapy, chemotherapy, and/or hormonal therapy, as per existing standard protocols
boolean
C0677850 (UMLS CUI [1,1])
C1442989 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
C1522449 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
C0279025 (UMLS CUI [4])
Neoplasm Metastasis Absent
Item
no detectable metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Pregnancy Absent
Item
not pregnant
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Able to speak English Language
Item
speaks english
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
Mental disorders Absent
Item
no history of mental illness
boolean
C0004936 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Prior Therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1])
ID.14
Item
see disease characteristics
boolean

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