Informationen:
Fehler:
ID
23643
Beschreibung
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
Stichworte
Versionen (1)
- 10.07.17 10.07.17 -
Hochgeladen am
10. Juli 2017
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00971919
Eligibility Breast Cancer NCT00971919
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00971919
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
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])
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])
C0474926 (UMLS CUI [1,2])
Disease Resectable
Item
resectable disease
boolean
C0012634 (UMLS CUI [1,1])
C1514888 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
C0332197 (UMLS CUI [1,2])
Able to speak English Language
Item
speaks english
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
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])
C0332197 (UMLS CUI [1,2])
Prior Therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1])
ID.14
Item
see disease characteristics
boolean