ID

35870

Description

Anesthesia and Circulating Tumor Cells in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02005770

Link

https://clinicaltrials.gov/show/NCT02005770

Keywords

Versions (1)
  1. 3/30/19 3/30/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 30, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Female Breast Carcinoma NCT02005770

English

Eligibility Female Breast Carcinoma NCT02005770

1 forms  
Criteria
Description

Criteria

age 18 to 85
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
asa i-iii
Description

ASA physical status classification

Data type

boolean

Alias
UMLS CUI [1]
C0450990
primary breast cancer (tnm stage = t1-3, n0-2, m0)
Description

Breast Carcinoma Primary TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C0474926
primary surgery
Description

Operative Surgical Procedures Primary

Data type

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0205225
written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic breast cancer
Description

Secondary malignant neoplasm of female breast

Data type

boolean

Alias
UMLS CUI [1]
C0346993
other than primary surgery (recurrence, reconstruction)
Description

Operative Surgical Procedures | Exception Operative Surgical Procedures Primary | Recurrence | Reconstructive Surgical Procedures

Data type

boolean

Alias
UMLS CUI [1]
C0543467
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0543467
UMLS CUI [2,3]
C0205225
UMLS CUI [3]
C0034897
UMLS CUI [4]
C0524865
pre-operative chemotherapy or radiotherapy
Description

Preoperative Chemotherapy | Preoperative course of radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C2347669
UMLS CUI [2]
C0436204
auto-immune disease, hiv, other active cancer, age>85, asa iv or v
Description

Autoimmune Disease | HIV Infection | Cancer Other | Age | ASA physical status classification

Data type

boolean

Alias
UMLS CUI [1]
C0004364
UMLS CUI [2]
C0019693
UMLS CUI [3]
C1707251
UMLS CUI [4]
C0001779
UMLS CUI [5]
C0450990
concomitant regional anesthesia
Description

Regional anesthesia

Data type

boolean

Alias
UMLS CUI [1]
C0002911
chronic opioids medication
Description

Opioids chronic

Data type

boolean

Alias
UMLS CUI [1,1]
C0242402
UMLS CUI [1,2]
C0205191
any systemic immunosuppressive therapy
Description

Therapeutic immunosuppression Systemic

Data type

boolean

Alias
UMLS CUI [1,1]
C0021079
UMLS CUI [1,2]
C0205373
known hypersensitivity or suspected allergy to propofol, soya or egg proteins
Description

Propofol allergy | Propofol allergy Suspected | Allergy to soy | Allergy to soy Suspected | Egg protein allergy | Egg protein allergy Suspected

Data type

boolean

Alias
UMLS CUI [1]
C0570632
UMLS CUI [2,1]
C0570632
UMLS CUI [2,2]
C0750491
UMLS CUI [3]
C4075590
UMLS CUI [4,1]
C4075590
UMLS CUI [4,2]
C0750491
UMLS CUI [5]
C0567447
UMLS CUI [6,1]
C0567447
UMLS CUI [6,2]
C0750491
known hypersensitivity to volatile anesthetics (malignant hyperthermia)
Description

Inhalational anesthetics allergy | Malignant hyperthermia

Data type

boolean

Alias
UMLS CUI [1]
C0570635
UMLS CUI [2]
C0024591
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
breast feeding
Description

Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0006147
non german-speaking patients
Description

Lacking Able to speak German language

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564215
UMLS CUI [1,3]
C0017477
enrollment in any other clinical trial during the course of this trial, 30 days prior to its beginning or 30 days after its completion
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Female Breast Carcinoma NCT02005770

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Age
Item
age 18 to 85
boolean
C0001779 (UMLS CUI [1])
ASA physical status classification
Item
asa i-iii
boolean
C0450990 (UMLS CUI [1])
Breast Carcinoma Primary TNM Breast tumor staging
Item
primary breast cancer (tnm stage = t1-3, n0-2, m0)
boolean
C0678222 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
Operative Surgical Procedures Primary
Item
primary surgery
boolean
C0543467 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Secondary malignant neoplasm of female breast
Item
metastatic breast cancer
boolean
C0346993 (UMLS CUI [1])
Operative Surgical Procedures | Exception Operative Surgical Procedures Primary | Recurrence | Reconstructive Surgical Procedures
Item
other than primary surgery (recurrence, reconstruction)
boolean
C0543467 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C0205225 (UMLS CUI [2,3])
C0034897 (UMLS CUI [3])
C0524865 (UMLS CUI [4])
Preoperative Chemotherapy | Preoperative course of radiotherapy
Item
pre-operative chemotherapy or radiotherapy
boolean
C2347669 (UMLS CUI [1])
C0436204 (UMLS CUI [2])
Autoimmune Disease | HIV Infection | Cancer Other | Age | ASA physical status classification
Item
auto-immune disease, hiv, other active cancer, age>85, asa iv or v
boolean
C0004364 (UMLS CUI [1])
C0019693 (UMLS CUI [2])
C1707251 (UMLS CUI [3])
C0001779 (UMLS CUI [4])
C0450990 (UMLS CUI [5])
Regional anesthesia
Item
concomitant regional anesthesia
boolean
C0002911 (UMLS CUI [1])
Opioids chronic
Item
chronic opioids medication
boolean
C0242402 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Therapeutic immunosuppression Systemic
Item
any systemic immunosuppressive therapy
boolean
C0021079 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
Propofol allergy | Propofol allergy Suspected | Allergy to soy | Allergy to soy Suspected | Egg protein allergy | Egg protein allergy Suspected
Item
known hypersensitivity or suspected allergy to propofol, soya or egg proteins
boolean
C0570632 (UMLS CUI [1])
C0570632 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C4075590 (UMLS CUI [3])
C4075590 (UMLS CUI [4,1])
C0750491 (UMLS CUI [4,2])
C0567447 (UMLS CUI [5])
C0567447 (UMLS CUI [6,1])
C0750491 (UMLS CUI [6,2])
Inhalational anesthetics allergy | Malignant hyperthermia
Item
known hypersensitivity to volatile anesthetics (malignant hyperthermia)
boolean
C0570635 (UMLS CUI [1])
C0024591 (UMLS CUI [2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
breast feeding
boolean
C0006147 (UMLS CUI [1])
Lacking Able to speak German language
Item
non german-speaking patients
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0017477 (UMLS CUI [1,3])
Study Subject Participation Status
Item
enrollment in any other clinical trial during the course of this trial, 30 days prior to its beginning or 30 days after its completion
boolean
C2348568 (UMLS CUI [1])
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