ID

44752

Descrizione

Lymph Node Mapping in Patients With Newly Diagnosed Endometrial Cancer Undergoing Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT01939028

collegamento

https://clinicaltrials.gov/show/NCT01939028

Keywords

versioni (1)
  1. 10/11/21 10/11/21 -
Titolare del copyright

Case Comprehensive Cancer Center

Caricato su

10 novembre 2021

DOI

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Licenza

Creative Commons BY-NC 4.0
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Eligibility Stage I Endometrial Carcinoma NCT01939028

Inglese

Eligibility Stage I Endometrial Carcinoma NCT01939028

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
women must have newly diagnosed histologically or cytologically confirmed endometrial cancer
Descrizione

women must have newly diagnosed histologically or cytologically confirmed endometrial cancer

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C0476089
UMLS CUI [1,3]
C1518321
UMLS CUI [1,4]
C0449575
UMLS CUI [2,1]
C0086287
UMLS CUI [2,2]
C0476089
UMLS CUI [2,3]
C1518321
UMLS CUI [2,4]
C0205471
women should have received no prior therapy for their disease
Descrizione

women should have received no prior therapy for their disease

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0332197
women who are planning to undergo hysterectomy, bilateral salpingo-oophorectomy, and pelvic lymphadenectomy for the management of their endometrial cancer
Descrizione

women who are planning to undergo hysterectomy, bilateral salpingo-oophorectomy, and pelvic lymphadenectomy for the management of their endometrial cancer

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C0020699
UMLS CUI [1,3]
C1301732
UMLS CUI [2,1]
C0086287
UMLS CUI [2,2]
C0195495
UMLS CUI [2,3]
C1301732
UMLS CUI [3,1]
C0086287
UMLS CUI [3,2]
C0193883
UMLS CUI [3,3]
C1301732
women must have the ability to understand and the willingness to sign a written informed consent document
Descrizione

women must have the ability to understand and the willingness to sign a written informed consent document

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0162340
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0600109
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
women who are receiving any other investigational agents
Descrizione

women who are receiving any other investigational agents

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0013230
UMLS CUI [1,4]
C0205394
women with a history of allergic reactions attributed to compounds of similar chemical or biologic composition to isosulfan blue or indocyanine green or other agents used in this study
Descrizione

women with a history of allergic reactions attributed to compounds of similar chemical or biologic composition to isosulfan blue or indocyanine green or other agents used in this study

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1527304
UMLS CUI [1,2]
C0063908
UMLS CUI [1,3]
C1706082
UMLS CUI [1,4]
C0486616
UMLS CUI [1,5]
C2348205
UMLS CUI [2,1]
C1527304
UMLS CUI [2,2]
C0021234
UMLS CUI [2,3]
C1706082
UMLS CUI [2,4]
C0486616
UMLS CUI [2,5]
C2348205
UMLS CUI [3,1]
C1527304
UMLS CUI [3,2]
C0205394
UMLS CUI [3,3]
C1521826
UMLS CUI [3,4]
C1706082
UMLS CUI [3,5]
C0486616
UMLS CUI [3,6]
C2348205
women with hypersensitivity to phenylmethane compounds, or a history of allergic reaction to iodides
Descrizione

women with hypersensitivity to phenylmethane compounds, or a history of allergic reaction to iodides

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C0020517
UMLS CUI [1,3]
C0650066
UMLS CUI [1,4]
C1706082
UMLS CUI [2,1]
C0262926
UMLS CUI [2,2]
C1527304
UMLS CUI [2,3]
C0021966
patients with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Descrizione

patients with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
UMLS CUI [1,3]
C0009450
UMLS CUI [1,4]
C0742758
UMLS CUI [1,5]
C0002965
UMLS CUI [1,6]
C0003811
UMLS CUI [1,7]
C0004936
UMLS CUI [1,8]
C0439801
UMLS CUI [1,9]
C0525058
UMLS CUI [1,10]
C0748872
women with a history of prior loop electrosurgical excision procedure (leep) or cone procedures performed on their cervix
Descrizione

women with a history of prior loop electrosurgical excision procedure (leep) or cone procedures performed on their cervix

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C4039811
UMLS CUI [1,3]
C1514463
UMLS CUI [1,4]
C0007874
UMLS CUI [2,1]
C0086287
UMLS CUI [2,2]
C0262926
UMLS CUI [2,3]
C0195324
UMLS CUI [2,4]
C0007874
women with a history of lymphedema, lymphoma, or lymphatic hyperplasia (castleman disease)
Descrizione

women with a history of lymphedema, lymphoma, or lymphatic hyperplasia (castleman disease)

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C0262926
UMLS CUI [1,3]
C0024236
UMLS CUI [2,1]
C0086287
UMLS CUI [2,2]
C0262926
UMLS CUI [2,3]
C0024299
UMLS CUI [3,1]
C0086287
UMLS CUI [3,2]
C0262926
UMLS CUI [3,3]
C0017531
women with a history of a prior malignancy
Descrizione

women with a history of a prior malignancy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0086287
UMLS CUI [1,2]
C0262926
UMLS CUI [1,3]
C0006826
women may also be excluded at the discretion of their surgeon if he or she feels that the patient is not an appropriate candidate
Descrizione

women may also be excluded at the discretion of their surgeon if he or she feels that the patient is not an appropriate candidate

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1302261
UMLS CUI [1,2]
C0008961
UMLS CUI [1,3]
C0022423
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Similar models

Eligibility Stage I Endometrial Carcinoma NCT01939028

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
women must have newly diagnosed histologically or cytologically confirmed endometrial cancer
Item
women must have newly diagnosed histologically or cytologically confirmed endometrial cancer
boolean
C0086287 (UMLS CUI [1,1])
C0476089 (UMLS CUI [1,2])
C1518321 (UMLS CUI [1,3])
C0449575 (UMLS CUI [1,4])
C0086287 (UMLS CUI [2,1])
C0476089 (UMLS CUI [2,2])
C1518321 (UMLS CUI [2,3])
C0205471 (UMLS CUI [2,4])
women should have received no prior therapy for their disease
Item
women should have received no prior therapy for their disease
boolean
C0086287 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
women who are planning to undergo hysterectomy, bilateral salpingo-oophorectomy, and pelvic lymphadenectomy for the management of their endometrial cancer
Item
women who are planning to undergo hysterectomy, bilateral salpingo-oophorectomy, and pelvic lymphadenectomy for the management of their endometrial cancer
boolean
C0086287 (UMLS CUI [1,1])
C0020699 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0086287 (UMLS CUI [2,1])
C0195495 (UMLS CUI [2,2])
C1301732 (UMLS CUI [2,3])
C0086287 (UMLS CUI [3,1])
C0193883 (UMLS CUI [3,2])
C1301732 (UMLS CUI [3,3])
women must have the ability to understand and the willingness to sign a written informed consent document
Item
women must have the ability to understand and the willingness to sign a written informed consent document
boolean
C0021430 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
women who are receiving any other investigational agents
Item
women who are receiving any other investigational agents
boolean
C0086287 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
women with a history of allergic reactions attributed to compounds of similar chemical or biologic composition to isosulfan blue or indocyanine green or other agents used in this study
Item
women with a history of allergic reactions attributed to compounds of similar chemical or biologic composition to isosulfan blue or indocyanine green or other agents used in this study
boolean
C1527304 (UMLS CUI [1,1])
C0063908 (UMLS CUI [1,2])
C1706082 (UMLS CUI [1,3])
C0486616 (UMLS CUI [1,4])
C2348205 (UMLS CUI [1,5])
C1527304 (UMLS CUI [2,1])
C0021234 (UMLS CUI [2,2])
C1706082 (UMLS CUI [2,3])
C0486616 (UMLS CUI [2,4])
C2348205 (UMLS CUI [2,5])
C1527304 (UMLS CUI [3,1])
C0205394 (UMLS CUI [3,2])
C1521826 (UMLS CUI [3,3])
C1706082 (UMLS CUI [3,4])
C0486616 (UMLS CUI [3,5])
C2348205 (UMLS CUI [3,6])
women with hypersensitivity to phenylmethane compounds, or a history of allergic reaction to iodides
Item
women with hypersensitivity to phenylmethane compounds, or a history of allergic reaction to iodides
boolean
C0086287 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0650066 (UMLS CUI [1,3])
C1706082 (UMLS CUI [1,4])
C0262926 (UMLS CUI [2,1])
C1527304 (UMLS CUI [2,2])
C0021966 (UMLS CUI [2,3])
patients with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Item
patients with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0009450 (UMLS CUI [1,3])
C0742758 (UMLS CUI [1,4])
C0002965 (UMLS CUI [1,5])
C0003811 (UMLS CUI [1,6])
C0004936 (UMLS CUI [1,7])
C0439801 (UMLS CUI [1,8])
C0525058 (UMLS CUI [1,9])
C0748872 (UMLS CUI [1,10])
women with a history of prior loop electrosurgical excision procedure (leep) or cone procedures performed on their cervix
Item
women with a history of prior loop electrosurgical excision procedure (leep) or cone procedures performed on their cervix
boolean
C0086287 (UMLS CUI [1,1])
C4039811 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,3])
C0007874 (UMLS CUI [1,4])
C0086287 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
C0195324 (UMLS CUI [2,3])
C0007874 (UMLS CUI [2,4])
women with a history of lymphedema, lymphoma, or lymphatic hyperplasia (castleman disease)
Item
women with a history of lymphedema, lymphoma, or lymphatic hyperplasia (castleman disease)
boolean
C0086287 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0024236 (UMLS CUI [1,3])
C0086287 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
C0024299 (UMLS CUI [2,3])
C0086287 (UMLS CUI [3,1])
C0262926 (UMLS CUI [3,2])
C0017531 (UMLS CUI [3,3])
women with a history of a prior malignancy
Item
women with a history of a prior malignancy
boolean
C0086287 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
women may also be excluded at the discretion of their surgeon if he or she feels that the patient is not an appropriate candidate
Item
women may also be excluded at the discretion of their surgeon if he or she feels that the patient is not an appropriate candidate
boolean
C1302261 (UMLS CUI [1,1])
C0008961 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,3])
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