ID

16380

Description

The Efficacy of Prophylactic Antibiotic Administration During Breast Cancer Surgery in Overweight Patients.; ODM derived from: https://clinicaltrials.gov/show/NCT00356148

Link

https://clinicaltrials.gov/show/NCT00356148

Keywords

  1. 7/13/16 7/13/16 -
  2. 7/13/16 7/13/16 -
Uploaded on

July 13, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00356148

Eligibility Breast Cancer NCT00356148

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
women at any age with early stage breast cancer (stage i-ii) and american society of anesthesiologists (asa) score of i-ii.
Description

Gender | Age | Early-Stage Breast Carcinoma | American Society of Anesthesiologists physical status classification

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
UMLS CUI [3]
C2986665
UMLS CUI [4]
C0450990
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
ductal carcinoma in situ (dcis; stage 0 cancer),
Description

Noninfiltrating Intraductal Carcinoma | Stage 0 Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0007124
UMLS CUI [2]
C0154084
advanced or distant metastatic stage,
Description

Advanced cancer | Metastatic Neoplasm Distant

Data type

boolean

Alias
UMLS CUI [1]
C0877373
UMLS CUI [2,1]
C2939420
UMLS CUI [2,2]
C0443203
receiving any neoadjuvant therapy,
Description

Neoadjuvant Therapy

Data type

boolean

Alias
UMLS CUI [1]
C0600558
history of receiving any antibiotics within prior 3 months,
Description

Antibiotics

Data type

boolean

Alias
UMLS CUI [1]
C0003232
history of immunodeficiency,
Description

Immunologic Deficiency Syndromes

Data type

boolean

Alias
UMLS CUI [1]
C0021051
having a remote infection,
Description

Communicable Disease

Data type

boolean

Alias
UMLS CUI [1]
C0009450
history of reaction to study antibiotics,
Description

Reaction Antibiotics Investigational

Data type

boolean

Alias
UMLS CUI [1,1]
C0443286
UMLS CUI [1,2]
C0003232
UMLS CUI [1,3]
C1517586
denial of signing the consent form.
Description

Informed Consent Refused

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116

Similar models

Eligibility Breast Cancer NCT00356148

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age | Early-Stage Breast Carcinoma | American Society of Anesthesiologists physical status classification
Item
women at any age with early stage breast cancer (stage i-ii) and american society of anesthesiologists (asa) score of i-ii.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C2986665 (UMLS CUI [3])
C0450990 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Noninfiltrating Intraductal Carcinoma | Stage 0 Breast Carcinoma
Item
ductal carcinoma in situ (dcis; stage 0 cancer),
boolean
C0007124 (UMLS CUI [1])
C0154084 (UMLS CUI [2])
Advanced cancer | Metastatic Neoplasm Distant
Item
advanced or distant metastatic stage,
boolean
C0877373 (UMLS CUI [1])
C2939420 (UMLS CUI [2,1])
C0443203 (UMLS CUI [2,2])
Neoadjuvant Therapy
Item
receiving any neoadjuvant therapy,
boolean
C0600558 (UMLS CUI [1])
Antibiotics
Item
history of receiving any antibiotics within prior 3 months,
boolean
C0003232 (UMLS CUI [1])
Immunologic Deficiency Syndromes
Item
history of immunodeficiency,
boolean
C0021051 (UMLS CUI [1])
Communicable Disease
Item
having a remote infection,
boolean
C0009450 (UMLS CUI [1])
Reaction Antibiotics Investigational
Item
history of reaction to study antibiotics,
boolean
C0443286 (UMLS CUI [1,1])
C0003232 (UMLS CUI [1,2])
C1517586 (UMLS CUI [1,3])
Informed Consent Refused
Item
denial of signing the consent form.
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])

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