Información:
Error:
ID
14619
Descripción
EF5 to Evaluate Tumor Hypoxia in Patients With High-Grade Soft Tissue Sarcoma or Mouth Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00896961
Link
https://clinicaltrials.gov/show/NCT00896961
Palabras clave
Versiones (1)
- 24.04.16 24.04.16 -
Subido en
24. April 2016
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Stage I Adult Soft Tissue Sarcoma NCT00896961
Eligibility Stage I Adult Soft Tissue Sarcoma NCT00896961
- StudyEvent: Eligibility
Similar models
Eligibility Stage I Adult Soft Tissue Sarcoma NCT00896961
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
soft tissue sarcoma or squamous cell carcinoma
Item
histologically confirmed high-grade soft tissue sarcoma (sts) of the trunk or extremity or squamous cell carcinoma of the oral cavity for which surgical biopsy or resection is standard initial therapy
boolean
C0334449 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0007137 (UMLS CUI [2,1])
C0226896 (UMLS CUI [2,2])
C0205082 (UMLS CUI [1,2])
C0007137 (UMLS CUI [2,1])
C0226896 (UMLS CUI [2,2])
clinical imaging
Item
clinical imaging of mass that is likely to be sts or squamous cell carcinoma of the head and neck allowed if surgery is indicated prior to definitive diagnosis
boolean
C0011923 (UMLS CUI [1])
resection and standard oncologic treatment
Item
planned resection and standard oncologic treatment
boolean
C0728940 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0205478 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,1])
C0205478 (UMLS CUI [2,2])
metastatic disease
Item
no known distant metastatic disease
boolean
C0027627 (UMLS CUI [1])
ECOG
Item
ecog 0-2
boolean
C1520224 (UMLS CUI [1])
WBC
Item
wbc at least 2,000/mm^3
boolean
C0023508 (UMLS CUI [1])
platelet count
Item
platelet count at least 100,000/mm^3
boolean
C0005821 (UMLS CUI [1])
bilirubin
Item
bilirubin less than 2.0 mg/dl
boolean
C1278039 (UMLS CUI [1])
creatinine
Item
creatinine less than 2.0 mg/dl or creatinine clearance at least 50 ml/min
boolean
C0201976 (UMLS CUI [1])
cardiac condition
Item
no significant cardiac condition that would preclude study compliance
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1842820 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C1842820 (UMLS CUI [1,3])
weight
Item
weight no greater than 130 kg
boolean
C0005910 (UMLS CUI [1])
peripheral neuropathy
Item
no grade iii or iv peripheral neuropathy
boolean
C0031117 (UMLS CUI [1])
medical condition that would preclude study compliance
Item
no other medical condition that would preclude study compliance
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
pregnancy or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
effective contraception
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1])
no chemotherapy within 3 months
Item
no chemotherapy within 3 months before planned surgery
boolean
C0392920 (UMLS CUI [1])
preoperative radiotherapy
Item
preoperative radiotherapy allowed for sts
boolean
C1522449 (UMLS CUI [1])
no radiotherapy within 3 months
Item
no radiotherapy within 3 months before planned surgery
boolean
C1522449 (UMLS CUI [1])
no other concurrent investigational agents
Item
no other concurrent investigational agents
boolean
C2348568 (UMLS CUI [1])