Eligibility Stage I Adult Soft Tissue Sarcoma NCT00896961

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
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
Beschrijving

soft tissue sarcoma or squamous cell carcinoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0334449
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0007137
UMLS CUI [2,2]
C0226896
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
Beschrijving

clinical imaging

Datatype

boolean

Alias
UMLS CUI [1]
C0011923
planned resection and standard oncologic treatment
Beschrijving

resection and standard oncologic treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0728940
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0205478
no known distant metastatic disease
Beschrijving

metastatic disease

Datatype

boolean

Alias
UMLS CUI [1]
C0027627
ecog 0-2
Beschrijving

ECOG

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
wbc at least 2,000/mm^3
Beschrijving

WBC

Datatype

boolean

Alias
UMLS CUI [1]
C0023508
platelet count at least 100,000/mm^3
Beschrijving

platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
bilirubin less than 2.0 mg/dl
Beschrijving

bilirubin

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
creatinine less than 2.0 mg/dl or creatinine clearance at least 50 ml/min
Beschrijving

creatinine

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
no significant cardiac condition that would preclude study compliance
Beschrijving

cardiac condition

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C1842820
weight no greater than 130 kg
Beschrijving

weight

Datatype

boolean

Alias
UMLS CUI [1]
C0005910
no grade iii or iv peripheral neuropathy
Beschrijving

peripheral neuropathy

Datatype

boolean

Alias
UMLS CUI [1]
C0031117
no other medical condition that would preclude study compliance
Beschrijving

medical condition that would preclude study compliance

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
not pregnant or nursing
Beschrijving

pregnancy or nursing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
fertile patients must use effective contraception
Beschrijving

effective contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
no chemotherapy within 3 months before planned surgery
Beschrijving

see disease characteristics

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
preoperative radiotherapy allowed for sts
Beschrijving

preoperative radiotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
no radiotherapy within 3 months before planned surgery
Beschrijving

no radiotherapy within 3 months

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
no other concurrent investigational agents
Beschrijving

no other concurrent investigational agents

Datatype

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Stage I Adult Soft Tissue Sarcoma NCT00896961

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
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])
pregnancy or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
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])