ID

13626

Description

Penclomedine in Treating Patients With Solid Tumors or Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00002946

Lien

https://clinicaltrials.gov/show/NCT00002946

Mots-clés

  1. 21/02/2016 21/02/2016 -
Téléchargé le

21 février 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Lymphoma NCT00002946

Eligibility Lymphoma NCT00002946

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00002946
Criteria
Description

Criteria

histologically confirmed malignancy (solid tumor or lymphoma)
Description

solid tumor or lymphoma

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0280100
UMLS CUI [3]
C0024299
no history of brain metastases
Description

brain metastases

Type de données

boolean

Alias
UMLS CUI [1]
C0220650
age: 18 and over
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
life expectancy: at least 12 weeks
Description

life expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
performance status: ecog 0-2
Description

performance status

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
wbc at least 4,000/mm3
Description

wbc

Type de données

boolean

Alias
UMLS CUI [1]
C0023508
absolute neutrophil count at least 1,500/mm3
Description

absolute neutrophil count

Type de données

boolean

Alias
UMLS CUI [1]
C0948762
platelet count at least 100,000/mm3
Description

platelet count

Type de données

boolean

Alias
UMLS CUI [1]
C0005821
bilirubin less than 1.5 mg/dl
Description

bilirubin

Type de données

boolean

Alias
UMLS CUI [1]
C1278039
creatinine normal
Description

creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
no history of seizure disorder not pregnant or nursing
Description

seizure disorder, pregnancy, breast feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0014544
UMLS CUI [2]
C0549206
UMLS CUI [3]
C0006147
at least 4 weeks since prior chemotherapy (6 weeks since nitrosoureas and mitomycin) and recovered
Description

prior chemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C1514463
UMLS CUI [2]
C0392920
at least 4 weeks since prior radiotherapy and recovered
Description

prior radiotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C1514463
UMLS CUI [2]
C1522449

Similar models

Eligibility Lymphoma NCT00002946

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00002946
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
solid tumor or lymphoma
Item
histologically confirmed malignancy (solid tumor or lymphoma)
boolean
C0006826 (UMLS CUI [1])
C0280100 (UMLS CUI [2])
C0024299 (UMLS CUI [3])
brain metastases
Item
no history of brain metastases
boolean
C0220650 (UMLS CUI [1])
age
Item
age: 18 and over
boolean
C0001779 (UMLS CUI [1])
life expectancy
Item
life expectancy: at least 12 weeks
boolean
C0023671 (UMLS CUI [1])
performance status
Item
performance status: ecog 0-2
boolean
C1520224 (UMLS CUI [1])
wbc
Item
wbc at least 4,000/mm3
boolean
C0023508 (UMLS CUI [1])
absolute neutrophil count
Item
absolute neutrophil count at least 1,500/mm3
boolean
C0948762 (UMLS CUI [1])
platelet count
Item
platelet count at least 100,000/mm3
boolean
C0005821 (UMLS CUI [1])
bilirubin
Item
bilirubin less than 1.5 mg/dl
boolean
C1278039 (UMLS CUI [1])
creatinine
Item
creatinine normal
boolean
C0201976 (UMLS CUI [1])
seizure disorder, pregnancy, breast feeding
Item
no history of seizure disorder not pregnant or nursing
boolean
C0014544 (UMLS CUI [1])
C0549206 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
prior chemotherapy
Item
at least 4 weeks since prior chemotherapy (6 weeks since nitrosoureas and mitomycin) and recovered
boolean
C1514463 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
prior radiotherapy
Item
at least 4 weeks since prior radiotherapy and recovered
boolean
C1514463 (UMLS CUI [1])
C1522449 (UMLS CUI [2])

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