ID

20199

Descrizione

A Phase III Trial Comparing UFT+PSK to UFT+LV in Stage IIB, III Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00385970

collegamento

https://clinicaltrials.gov/show/NCT00385970

Keywords

versioni (1)
  1. 12/02/17 12/02/17 -
Caricato su

12 febbraio 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
Commenti del modello :

Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.

Torna ai commenti del modello
Commenti del gruppo di articoli per :

Commenti dell'articolo per :

Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.

Eligibility Colorectal Cancer NCT00385970

Inglese

Eligibility Colorectal Cancer NCT00385970

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with ptnm stage iib or iii (uicc sixth version) primary colon cancer/rectal cancer who have undergone surgery of histological curability a (including laparoscopic surgery) (the curability is judged after surgery)
Descrizione

Colon Carcinoma Primary TNM clinical staging | Rectal Carcinoma Primary TNM clinical staging | Operative Surgical Procedure Cure Histologic | Surgical Procedures, Laparoscopic

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0699790
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C3258246
UMLS CUI [2,1]
C0007113
UMLS CUI [2,2]
C0205225
UMLS CUI [2,3]
C3258246
UMLS CUI [3,1]
C0543467
UMLS CUI [3,2]
C1880198
UMLS CUI [3,3]
C0205462
UMLS CUI [4]
C0751429
patients with primary tumor that directly invades other organs or structures and/or perforates into the visceral peritoneum (t4) or with histologically positive lymph node metastasis (n+) (to be judged after surgery)
Descrizione

Primary tumor Visceral Peritoneum TNM clinical staging | Secondary malignant neoplasm of lymph node Histologic Positive

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0230206
UMLS CUI [1,3]
C3258246
UMLS CUI [2,1]
C0686619
UMLS CUI [2,2]
C0205462
UMLS CUI [2,3]
C1514241
patients who is between 20 and 80 years old at the time of obtaining informed consent
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
patients with performance status of 0 - 2
Descrizione

performance status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1518965
patients without receiving any cancer treatment such as radiation, chemotherapy, and immunotherapy before surgical operation
Descrizione

cancer treatment Absent | Therapeutic radiology procedure | Chemotherapy | Immunotherapy | Operative Surgical Procedures

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0332197
UMLS CUI [2]
C1522449
UMLS CUI [3]
C0392920
UMLS CUI [4]
C0021083
UMLS CUI [5]
C0543467
patients without severe dysfunction of renal, hepatic, or bone marrow function
Descrizione

Renal dysfunction Severe Absent | Liver Dysfunction Severe Absent | Bone Marrow Dysfunction Severe Absent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3279454
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C0086565
UMLS CUI [2,2]
C0205082
UMLS CUI [2,3]
C0332197
UMLS CUI [3,1]
C0005953
UMLS CUI [3,2]
C3887504
UMLS CUI [3,3]
C0205082
UMLS CUI [3,4]
C0332197
patients without serious complications such as bone marrow suppression, diarrhea, and infections diseases
Descrizione

Complication Serious Absent | Bone Marrow Suppression | Diarrhea | Communicable Diseases

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0332197
UMLS CUI [2]
C0280962
UMLS CUI [3]
C0011991
UMLS CUI [4]
C0009450
patients who have given consent to participate in this clinical study by himself/herself or his/her family
Descrizione

Informed Consent | Informed Consent Family

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0015576
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients in whom the bottom of tumor reaches the peritoneal reflection
Descrizione

Malignant Neoplasm Bottom Peritoneum

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C1511276
UMLS CUI [1,3]
C0031153
patients with lower rectal cancer (rb), anal canal (p), or circumanal skin (e)
Descrizione

Rectal Carcinoma Lower | Malignant neoplasm of anal canal | Malignant Neoplasms Perianal skin

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0007113
UMLS CUI [1,2]
C0441994
UMLS CUI [2]
C0153445
UMLS CUI [3,1]
C0006826
UMLS CUI [3,2]
C1704244
patients who has active multiple cancers or whose disease-free survival is less than 5 years even though the cancers are metachronous (except carcinoma in situ and skin cancers)
Descrizione

Multiple malignancy | Life Expectancy Disease Free of | Malignant Neoplasms Timepoint Different | Carcinoma in Situ | Skin carcinoma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0346429
UMLS CUI [2,1]
C0023671
UMLS CUI [2,2]
C0012634
UMLS CUI [2,3]
C0332296
UMLS CUI [3,1]
C0006826
UMLS CUI [3,2]
C2348792
UMLS CUI [3,3]
C1705242
UMLS CUI [4]
C0007099
UMLS CUI [5]
C0699893
women who are currently pregnant or wish to be pregnant during this clinical study
Descrizione

Pregnancy | Pregnancy, Planned

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
patients who are judged to be inappropriate to participate in this clinical study by the investigator or subinvestigator
Descrizione

Study Subject Participation Status Inappropriate

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
Ritorna all'inizio della pagina

Similar models

Eligibility Colorectal Cancer NCT00385970

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Colon Carcinoma Primary TNM clinical staging | Rectal Carcinoma Primary TNM clinical staging | Operative Surgical Procedure Cure Histologic | Surgical Procedures, Laparoscopic
Item
patients with ptnm stage iib or iii (uicc sixth version) primary colon cancer/rectal cancer who have undergone surgery of histological curability a (including laparoscopic surgery) (the curability is judged after surgery)
boolean
C0699790 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0007113 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C0543467 (UMLS CUI [3,1])
C1880198 (UMLS CUI [3,2])
C0205462 (UMLS CUI [3,3])
C0751429 (UMLS CUI [4])
Primary tumor Visceral Peritoneum TNM clinical staging | Secondary malignant neoplasm of lymph node Histologic Positive
Item
patients with primary tumor that directly invades other organs or structures and/or perforates into the visceral peritoneum (t4) or with histologically positive lymph node metastasis (n+) (to be judged after surgery)
boolean
C0677930 (UMLS CUI [1,1])
C0230206 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0686619 (UMLS CUI [2,1])
C0205462 (UMLS CUI [2,2])
C1514241 (UMLS CUI [2,3])
Age
Item
patients who is between 20 and 80 years old at the time of obtaining informed consent
boolean
C0001779 (UMLS CUI [1])
performance status
Item
patients with performance status of 0 - 2
boolean
C1518965 (UMLS CUI [1])
cancer treatment Absent | Therapeutic radiology procedure | Chemotherapy | Immunotherapy | Operative Surgical Procedures
Item
patients without receiving any cancer treatment such as radiation, chemotherapy, and immunotherapy before surgical operation
boolean
C0920425 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
C0021083 (UMLS CUI [4])
C0543467 (UMLS CUI [5])
Renal dysfunction Severe Absent | Liver Dysfunction Severe Absent | Bone Marrow Dysfunction Severe Absent
Item
patients without severe dysfunction of renal, hepatic, or bone marrow function
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0086565 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0005953 (UMLS CUI [3,1])
C3887504 (UMLS CUI [3,2])
C0205082 (UMLS CUI [3,3])
C0332197 (UMLS CUI [3,4])
Complication Serious Absent | Bone Marrow Suppression | Diarrhea | Communicable Diseases
Item
patients without serious complications such as bone marrow suppression, diarrhea, and infections diseases
boolean
C0009566 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0280962 (UMLS CUI [2])
C0011991 (UMLS CUI [3])
C0009450 (UMLS CUI [4])
Informed Consent | Informed Consent Family
Item
patients who have given consent to participate in this clinical study by himself/herself or his/her family
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0015576 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Malignant Neoplasm Bottom Peritoneum
Item
patients in whom the bottom of tumor reaches the peritoneal reflection
boolean
C0006826 (UMLS CUI [1,1])
C1511276 (UMLS CUI [1,2])
C0031153 (UMLS CUI [1,3])
Rectal Carcinoma Lower | Malignant neoplasm of anal canal | Malignant Neoplasms Perianal skin
Item
patients with lower rectal cancer (rb), anal canal (p), or circumanal skin (e)
boolean
C0007113 (UMLS CUI [1,1])
C0441994 (UMLS CUI [1,2])
C0153445 (UMLS CUI [2])
C0006826 (UMLS CUI [3,1])
C1704244 (UMLS CUI [3,2])
Multiple malignancy | Life Expectancy Disease Free of | Malignant Neoplasms Timepoint Different | Carcinoma in Situ | Skin carcinoma
Item
patients who has active multiple cancers or whose disease-free survival is less than 5 years even though the cancers are metachronous (except carcinoma in situ and skin cancers)
boolean
C0346429 (UMLS CUI [1])
C0023671 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])
C0332296 (UMLS CUI [2,3])
C0006826 (UMLS CUI [3,1])
C2348792 (UMLS CUI [3,2])
C1705242 (UMLS CUI [3,3])
C0007099 (UMLS CUI [4])
C0699893 (UMLS CUI [5])
Pregnancy | Pregnancy, Planned
Item
women who are currently pregnant or wish to be pregnant during this clinical study
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
patients who are judged to be inappropriate to participate in this clinical study by the investigator or subinvestigator
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
Ritorna all'inizio della pagina 

Contatto

Si prega di utilizzare questo modulo per feedback, domande e suggerimenti per miglioramenti.

I campi contrassegnati da * sono obbligatori.

Aiuto

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial