ID

37699

Descrizione

Adjuvant Radiation for High Risk Bladder Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01954173

collegamento

https://clinicaltrials.gov/show/NCT01954173

Keywords

  1. 18/08/19 18/08/19 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

18 agosto 2019

DOI

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Licenza

Creative Commons BY 4.0

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Eligibility Bladder Cancer NCT01954173

Eligibility Bladder Cancer NCT01954173

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologic diagnosis of urothelial or squamous cell carcinoma of the bladder
Descrizione

Transitional cell carcinoma of bladder | Bladder Squamous Cell Carcinoma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0279680
UMLS CUI [2]
C0279681
patients must have undergone cystectomy (total cystectomy, radical cystectomy +/-
Descrizione

Cystectomy | Complete cystectomy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0010651
UMLS CUI [2]
C0194401
pelvic lymph node dissection) with no evidence of macroscopic residual disease
Descrizione

Pelvic lymphadenectomy | Residual disease Macroscopic Absent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0193883
UMLS CUI [2,1]
C0543478
UMLS CUI [2,2]
C0439806
UMLS CUI [2,3]
C0332197
eastern cooperative oncology group (ecog)/zubrod performance status of 0-2
Descrizione

ECOG performance status | Zubrod Performance Status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1520224
UMLS CUI [2]
C3714786
patients treated with simple cystectomy with macroscopically negative margins are eligible for this study
Descrizione

Simple cystectomy | Negative Surgical Margin Macroscopic

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0401447
UMLS CUI [2,1]
C1709157
UMLS CUI [2,2]
C0439806
clinical t-stage (prior to systemic therapy, if applicable) ≥ t3a and/or positive lymph nodes by transurethral resection of bladder tumor (turbt)/magnetic resonance imaging (mri)/computed tomography (ct)/positron emission tomography (pet)-ct or pathologic t-stage ≥ t3a and/or positive lymph nodes
Descrizione

Status pre- Systemic therapy | TNM clinical staging | Lymph nodes positive | Transurethral resection of bladder neoplasm | Magnetic Resonance Imaging | CT | PET/CT | Pathologic TNM stage

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0332152
UMLS CUI [1,2]
C1515119
UMLS CUI [2]
C3258246
UMLS CUI [3]
C0746319
UMLS CUI [4]
C0401496
UMLS CUI [5]
C0024485
UMLS CUI [6]
C0040405
UMLS CUI [7]
C1699633
UMLS CUI [8]
C1319019
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with metastatic disease outside of the pelvis
Descrizione

Neoplasm Metastasis | Exception Pelvis

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0027627
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0030797
prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years
Descrizione

Invasive cancer | Exception Skin carcinoma | Exception Disease Free Duration

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0677898
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0012634
UMLS CUI [3,3]
C0332296
UMLS CUI [3,4]
C0449238
prior radiation therapy to the pelvis
Descrizione

Radiotherapy to pelvis

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1536155
patients with active inflammatory bowel disease
Descrizione

Inflammatory Bowel Disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021390
severe acute co-morbidity, defined as follows:
Descrizione

Comorbidity Severe

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
unstable angina and/or congestive heart failure requiring hospitalization in the last 3 months
Descrizione

Angina, Unstable | Congestive heart failure Hospitalization Required

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2,1]
C0018802
UMLS CUI [2,2]
C1708385
transmural myocardial infarction within the last 6 months
Descrizione

Transmural myocardial infarction

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1400513
acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
Descrizione

Bacterial Infections | Mycoses | Requirement Antibiotics Intravenous

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0004623
UMLS CUI [2]
C0026946
UMLS CUI [3,1]
C1514873
UMLS CUI [3,2]
C0003232
UMLS CUI [3,3]
C1522726
chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration
Descrizione

Chronic obstructive pulmonary disease exacerbation Hospitalization Required | Chronic obstructive pulmonary disease exacerbation Excludes Investigational Therapy | Respiration Disorder Hospitalization Required | Respiration Disorder Excludes Investigational Therapy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3508933
UMLS CUI [1,2]
C1708385
UMLS CUI [2,1]
C3508933
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C0949266
UMLS CUI [3,1]
C0035204
UMLS CUI [3,2]
C1708385
UMLS CUI [4,1]
C0035204
UMLS CUI [4,2]
C0332196
UMLS CUI [4,3]
C0949266
acquired immune deficiency syndrome (aids) based upon current centers for disease control and prevention (cdc) definition; note, however, that human immunodeficiency virus (hiv) testing is not required for entry into this protocol; the need to exclude patients with aids from this protocol is necessary because the treatment involved in this protocol may be significantly immunosuppressive; protocol-specific requirements may also exclude immunocompromised patients
Descrizione

AIDS | Immunocompromised patients

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001175
UMLS CUI [2]
C0085393

Similar models

Eligibility Bladder Cancer NCT01954173

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Transitional cell carcinoma of bladder | Bladder Squamous Cell Carcinoma
Item
pathologic diagnosis of urothelial or squamous cell carcinoma of the bladder
boolean
C0279680 (UMLS CUI [1])
C0279681 (UMLS CUI [2])
Cystectomy | Complete cystectomy
Item
patients must have undergone cystectomy (total cystectomy, radical cystectomy +/-
boolean
C0010651 (UMLS CUI [1])
C0194401 (UMLS CUI [2])
Pelvic lymphadenectomy | Residual disease Macroscopic Absent
Item
pelvic lymph node dissection) with no evidence of macroscopic residual disease
boolean
C0193883 (UMLS CUI [1])
C0543478 (UMLS CUI [2,1])
C0439806 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
ECOG performance status | Zubrod Performance Status
Item
eastern cooperative oncology group (ecog)/zubrod performance status of 0-2
boolean
C1520224 (UMLS CUI [1])
C3714786 (UMLS CUI [2])
Simple cystectomy | Negative Surgical Margin Macroscopic
Item
patients treated with simple cystectomy with macroscopically negative margins are eligible for this study
boolean
C0401447 (UMLS CUI [1])
C1709157 (UMLS CUI [2,1])
C0439806 (UMLS CUI [2,2])
Status pre- Systemic therapy | TNM clinical staging | Lymph nodes positive | Transurethral resection of bladder neoplasm | Magnetic Resonance Imaging | CT | PET/CT | Pathologic TNM stage
Item
clinical t-stage (prior to systemic therapy, if applicable) ≥ t3a and/or positive lymph nodes by transurethral resection of bladder tumor (turbt)/magnetic resonance imaging (mri)/computed tomography (ct)/positron emission tomography (pet)-ct or pathologic t-stage ≥ t3a and/or positive lymph nodes
boolean
C0332152 (UMLS CUI [1,1])
C1515119 (UMLS CUI [1,2])
C3258246 (UMLS CUI [2])
C0746319 (UMLS CUI [3])
C0401496 (UMLS CUI [4])
C0024485 (UMLS CUI [5])
C0040405 (UMLS CUI [6])
C1699633 (UMLS CUI [7])
C1319019 (UMLS CUI [8])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis | Exception Pelvis
Item
patients with metastatic disease outside of the pelvis
boolean
C0027627 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0030797 (UMLS CUI [2,2])
Invasive cancer | Exception Skin carcinoma | Exception Disease Free Duration
Item
prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years
boolean
C0677898 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0012634 (UMLS CUI [3,2])
C0332296 (UMLS CUI [3,3])
C0449238 (UMLS CUI [3,4])
Radiotherapy to pelvis
Item
prior radiation therapy to the pelvis
boolean
C1536155 (UMLS CUI [1])
Inflammatory Bowel Disease
Item
patients with active inflammatory bowel disease
boolean
C0021390 (UMLS CUI [1])
Comorbidity Severe
Item
severe acute co-morbidity, defined as follows:
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Angina, Unstable | Congestive heart failure Hospitalization Required
Item
unstable angina and/or congestive heart failure requiring hospitalization in the last 3 months
boolean
C0002965 (UMLS CUI [1])
C0018802 (UMLS CUI [2,1])
C1708385 (UMLS CUI [2,2])
Transmural myocardial infarction
Item
transmural myocardial infarction within the last 6 months
boolean
C1400513 (UMLS CUI [1])
Bacterial Infections | Mycoses | Requirement Antibiotics Intravenous
Item
acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
boolean
C0004623 (UMLS CUI [1])
C0026946 (UMLS CUI [2])
C1514873 (UMLS CUI [3,1])
C0003232 (UMLS CUI [3,2])
C1522726 (UMLS CUI [3,3])
Chronic obstructive pulmonary disease exacerbation Hospitalization Required | Chronic obstructive pulmonary disease exacerbation Excludes Investigational Therapy | Respiration Disorder Hospitalization Required | Respiration Disorder Excludes Investigational Therapy
Item
chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration
boolean
C3508933 (UMLS CUI [1,1])
C1708385 (UMLS CUI [1,2])
C3508933 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0949266 (UMLS CUI [2,3])
C0035204 (UMLS CUI [3,1])
C1708385 (UMLS CUI [3,2])
C0035204 (UMLS CUI [4,1])
C0332196 (UMLS CUI [4,2])
C0949266 (UMLS CUI [4,3])
AIDS | Immunocompromised patients
Item
acquired immune deficiency syndrome (aids) based upon current centers for disease control and prevention (cdc) definition; note, however, that human immunodeficiency virus (hiv) testing is not required for entry into this protocol; the need to exclude patients with aids from this protocol is necessary because the treatment involved in this protocol may be significantly immunosuppressive; protocol-specific requirements may also exclude immunocompromised patients
boolean
C0001175 (UMLS CUI [1])
C0085393 (UMLS CUI [2])

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