ID

34662

Descripción

CO2 Laser and Open Surgery for T1N0 Glottic SCC With Anterior Commissure Involved; ODM derived from: https://clinicaltrials.gov/show/NCT02303457

Link

https://clinicaltrials.gov/show/NCT02303457

Palabras clave

Versiones (1)
  1. 22/1/19 22/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

22 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Squamous Cell Carcinoma of Glottis NCT02303457

Inglés

Eligibility Squamous Cell Carcinoma of Glottis NCT02303457

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
t1n0 scc of glottic carcinoma with anterior commissure involve
Descripción

Glottic Squamous Cell Carcinoma TNM clinical staging | Involvement Anterior commissure of larynx

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0280325
UMLS CUI [1,2]
C3258246
UMLS CUI [2,1]
C1314939
UMLS CUI [2,2]
C0225578
no nodal metastasis and distant metastasis
Descripción

Secondary malignant neoplasm of lymph node Absent | Distant metastasis Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0686619
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C1269798
UMLS CUI [2,2]
C0332197
all patients must have ct/mr and electronic laryngoscope test before surgery and after surgery
Descripción

CT Preoperative | CT Postoperative | MRI Preoperative | MRI Postoperative | Laryngoscopy Electronic Preoperative | Laryngoscopy Electronic Postoperative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0040405
UMLS CUI [1,2]
C0445204
UMLS CUI [2,1]
C0040405
UMLS CUI [2,2]
C0032790
UMLS CUI [3,1]
C0024485
UMLS CUI [3,2]
C0445204
UMLS CUI [4,1]
C0024485
UMLS CUI [4,2]
C0032790
UMLS CUI [5,1]
C0023072
UMLS CUI [5,2]
C0013850
UMLS CUI [5,3]
C0445204
UMLS CUI [6,1]
C0023072
UMLS CUI [6,2]
C0013850
UMLS CUI [6,3]
C0032790
expected lifetime>1 year
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
patients and families agreed to participate in the test and sign the informed consent
Descripción

Informed Consent | Informed Consent Family

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0015576
without cognitive impairment.
Descripción

Impaired cognition Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0338656
UMLS CUI [1,2]
C0332197
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
with severe cardiac insufficiency liver and kidney function is not complete systemic infection patients
Descripción

Heart failure Severe | Liver Dysfunction | Impaired kidney function | Sepsis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0086565
UMLS CUI [3]
C0184571
UMLS CUI [4]
C0243026
patients with pregnancy and lactation
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
have surgery contraindications
Descripción

Medical contraindication Operative Surgical Procedures

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0543467
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Similar models

Eligibility Squamous Cell Carcinoma of Glottis NCT02303457

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Glottic Squamous Cell Carcinoma TNM clinical staging | Involvement Anterior commissure of larynx
Item
t1n0 scc of glottic carcinoma with anterior commissure involve
boolean
C0280325 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C1314939 (UMLS CUI [2,1])
C0225578 (UMLS CUI [2,2])
Secondary malignant neoplasm of lymph node Absent | Distant metastasis Absent
Item
no nodal metastasis and distant metastasis
boolean
C0686619 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1269798 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
CT Preoperative | CT Postoperative | MRI Preoperative | MRI Postoperative | Laryngoscopy Electronic Preoperative | Laryngoscopy Electronic Postoperative
Item
all patients must have ct/mr and electronic laryngoscope test before surgery and after surgery
boolean
C0040405 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C0040405 (UMLS CUI [2,1])
C0032790 (UMLS CUI [2,2])
C0024485 (UMLS CUI [3,1])
C0445204 (UMLS CUI [3,2])
C0024485 (UMLS CUI [4,1])
C0032790 (UMLS CUI [4,2])
C0023072 (UMLS CUI [5,1])
C0013850 (UMLS CUI [5,2])
C0445204 (UMLS CUI [5,3])
C0023072 (UMLS CUI [6,1])
C0013850 (UMLS CUI [6,2])
C0032790 (UMLS CUI [6,3])
Life Expectancy
Item
expected lifetime>1 year
boolean
C0023671 (UMLS CUI [1])
Informed Consent | Informed Consent Family
Item
patients and families agreed to participate in the test and sign the informed consent
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0015576 (UMLS CUI [2,2])
Impaired cognition Absent
Item
without cognitive impairment.
boolean
C0338656 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Heart failure Severe | Liver Dysfunction | Impaired kidney function | Sepsis
Item
with severe cardiac insufficiency liver and kidney function is not complete systemic infection patients
boolean
C0018801 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0086565 (UMLS CUI [2])
C0184571 (UMLS CUI [3])
C0243026 (UMLS CUI [4])
Pregnancy | Breast Feeding
Item
patients with pregnancy and lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Medical contraindication Operative Surgical Procedures
Item
have surgery contraindications
boolean
C1301624 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
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