ID

22177

Description

A Feasibility Study of Oral Adjuvant Chemotherapy With S-1; ODM derived from: https://clinicaltrials.gov/show/NCT01459185

Lien

https://clinicaltrials.gov/show/NCT01459185

Mots-clés

  1. 21/05/2017 21/05/2017 -
  2. 22/05/2017 22/05/2017 -
Téléchargé le

22 mai 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Non-small Cell Lung Cancer NCT01459185

Eligibility Non-small Cell Lung Cancer NCT01459185

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. nsclc with histological proof.
Description

Non-Small Cell Lung Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0007131
2. pathological stage ib, ii, or iiia nsclc (fifth edition of uicc/ajcc 1997) after complete resection.
Description

Non-Small Cell Lung Carcinoma TNM clinical staging Post Complete excision

Type de données

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C3258246
UMLS CUI [1,3]
C0687676
UMLS CUI [1,4]
C0015250
3. no prior treatment except for surgery.
Description

Therapy naive | Operative Surgical Procedures

Type de données

boolean

Alias
UMLS CUI [1]
C0919936
UMLS CUI [2]
C0543467
4. sufficient oral intake.
Description

Oral food intake Sufficient

Type de données

boolean

Alias
UMLS CUI [1,1]
C0518037
UMLS CUI [1,2]
C0205410
5. performance status (ps) 0 or 1.
Description

performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1518965
6. patients also had to have adequate organ function (3500 <leukocytes < 12,000/mm3; thrombocytes, >100,000/mm3; total bilirubin,<1.5 mg/dl; ast and alt, less than twice the normal limits at each institution; bun, <25 mg/dl; creatinine, less than the normal limits at each institution; and creatinine clearance (ccr))
Description

Organ function | White Blood Cell Count procedure | Platelet Count measurement | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Blood urea nitrogen measurement | Creatinine measurement, serum | Creatinine clearance measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2]
C0023508
UMLS CUI [3]
C0032181
UMLS CUI [4]
C1278039
UMLS CUI [5]
C0201899
UMLS CUI [6]
C0201836
UMLS CUI [7]
C0005845
UMLS CUI [8]
C0201976
UMLS CUI [9]
C0373595
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. history of drug hypersensitivity.
Description

Drug Allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0013182
2. contraindication of oral s-1 administration (refer appended paper).
Description

Medical contraindication S-1 Oral

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0879262
UMLS CUI [1,3]
C1527415
3. serious surgical or non-surgical complications
Description

Complication of surgical procedure Serious | Complication Serious

Type de données

boolean

Alias
UMLS CUI [1,1]
C0274311
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C0009566
UMLS CUI [2,2]
C0205404
4. active secondary cancer.
Description

Secondary Malignant Neoplasm

Type de données

boolean

Alias
UMLS CUI [1]
C3266877
5. watery diarrhea.
Description

Watery diarrhoea

Type de données

boolean

Alias
UMLS CUI [1]
C0239182
6. pregnant or lactating women.
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
7. male who has intention to make pregnant
Description

Gender Intent Reproduction

Type de données

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C1283828
UMLS CUI [1,3]
C0035150
8. patient to whom primary doctor judged inadequate to register.
Description

Study Subject Participation Status Inadequate

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0205412

Similar models

Eligibility Non-small Cell Lung Cancer NCT01459185

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma
Item
1. nsclc with histological proof.
boolean
C0007131 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma TNM clinical staging Post Complete excision
Item
2. pathological stage ib, ii, or iiia nsclc (fifth edition of uicc/ajcc 1997) after complete resection.
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C0015250 (UMLS CUI [1,4])
Therapy naive | Operative Surgical Procedures
Item
3. no prior treatment except for surgery.
boolean
C0919936 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
Oral food intake Sufficient
Item
4. sufficient oral intake.
boolean
C0518037 (UMLS CUI [1,1])
C0205410 (UMLS CUI [1,2])
performance status
Item
5. performance status (ps) 0 or 1.
boolean
C1518965 (UMLS CUI [1])
Organ function | White Blood Cell Count procedure | Platelet Count measurement | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Blood urea nitrogen measurement | Creatinine measurement, serum | Creatinine clearance measurement
Item
6. patients also had to have adequate organ function (3500 <leukocytes < 12,000/mm3; thrombocytes, >100,000/mm3; total bilirubin,<1.5 mg/dl; ast and alt, less than twice the normal limits at each institution; bun, <25 mg/dl; creatinine, less than the normal limits at each institution; and creatinine clearance (ccr))
boolean
C0678852 (UMLS CUI [1])
C0023508 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
C1278039 (UMLS CUI [4])
C0201899 (UMLS CUI [5])
C0201836 (UMLS CUI [6])
C0005845 (UMLS CUI [7])
C0201976 (UMLS CUI [8])
C0373595 (UMLS CUI [9])
Item Group
C0680251 (UMLS CUI)
Drug Allergy
Item
1. history of drug hypersensitivity.
boolean
C0013182 (UMLS CUI [1])
Medical contraindication S-1 Oral
Item
2. contraindication of oral s-1 administration (refer appended paper).
boolean
C1301624 (UMLS CUI [1,1])
C0879262 (UMLS CUI [1,2])
C1527415 (UMLS CUI [1,3])
Complication of surgical procedure Serious | Complication Serious
Item
3. serious surgical or non-surgical complications
boolean
C0274311 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
Secondary Malignant Neoplasm
Item
4. active secondary cancer.
boolean
C3266877 (UMLS CUI [1])
Watery diarrhoea
Item
5. watery diarrhea.
boolean
C0239182 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
6. pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Gender Intent Reproduction
Item
7. male who has intention to make pregnant
boolean
C0079399 (UMLS CUI [1,1])
C1283828 (UMLS CUI [1,2])
C0035150 (UMLS CUI [1,3])
Study Subject Participation Status Inadequate
Item
8. patient to whom primary doctor judged inadequate to register.
boolean
C2348568 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

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