ID

31070

Description

Pilot Trial of Intravenous Vitamin C in Refractory Non-Hodgkin Lymphoma (NHL); ODM derived from: https://clinicaltrials.gov/show/NCT00626444

Link

https://clinicaltrials.gov/show/NCT00626444

Keywords

  1. 7/17/18 7/17/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

July 17, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Non-Hodgkin Lymphoma NCT00626444

Eligibility Non-Hodgkin Lymphoma NCT00626444

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age greater than 18 years old
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
aggressive or very aggressive nhl
Description

Aggressive NHL | Aggressive NHL Very

Data type

boolean

Alias
UMLS CUI [1]
C1332225
UMLS CUI [2,1]
C1332225
UMLS CUI [2,2]
C0442824
failed one or more therapies
Description

Therapeutic procedure Quantity failed

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0231175
patients must not have progressed within 60 days of last therapy
Description

Disease Progression Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0242656
UMLS CUI [1,2]
C0332197
not received allogeneic stem cell transplant
Description

Allogeneic hematopoietic stem cell transplant Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C4255274
UMLS CUI [1,2]
C0332197
no reasonable standard therapeutic options available
Description

Standard therapy Options Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C2936643
UMLS CUI [1,2]
C1518601
UMLS CUI [1,3]
C0332268
glucose 6 phosphate dehydrogenase status normal
Description

Glucose-6-phosphate dehydrogenase normal

Data type

boolean

Alias
UMLS CUI [1]
C1167968
ecog performance status 0-2
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
normal creatinine and transaminase
Description

Serum creatinine normal | Transaminases Normal

Data type

boolean

Alias
UMLS CUI [1]
C0438244
UMLS CUI [2,1]
C0002594
UMLS CUI [2,2]
C0205307
women of child-bearing potential confirm negative pregnancy test
Description

Childbearing Potential Pregnancy test negative

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0427780
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
significant co-morbid disorders
Description

Comorbidity Significant

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0750502
significant psychiatric symptoms
Description

Psychiatric symptom Significant

Data type

boolean

Alias
UMLS CUI [1,1]
C0233401
UMLS CUI [1,2]
C0750502
smoking
Description

Tobacco use

Data type

boolean

Alias
UMLS CUI [1]
C0543414
excessive alcohol or drug use
Description

Alcohol intake above recommended sensible limits | Drug use Excessive

Data type

boolean

Alias
UMLS CUI [1]
C0560219
UMLS CUI [2,1]
C2239127
UMLS CUI [2,2]
C0442802
enrollment in other experimental therapy
Description

Study Subject Participation Status | Therapy, Investigational

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0949266
active infection
Description

Communicable Disease

Data type

boolean

Alias
UMLS CUI [1]
C0009450
patients experiencing ongoing response to recent treatments
Description

Disease Response | Therapeutic procedure Recent

Data type

boolean

Alias
UMLS CUI [1]
C1704632
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0332185
patients who have received chemotherapy within 30 days or biological therapy within 6 weeks
Description

Chemotherapy | Biological treatment

Data type

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1531518

Similar models

Eligibility Non-Hodgkin Lymphoma NCT00626444

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age greater than 18 years old
boolean
C0001779 (UMLS CUI [1])
Aggressive NHL | Aggressive NHL Very
Item
aggressive or very aggressive nhl
boolean
C1332225 (UMLS CUI [1])
C1332225 (UMLS CUI [2,1])
C0442824 (UMLS CUI [2,2])
Therapeutic procedure Quantity failed
Item
failed one or more therapies
boolean
C0087111 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Disease Progression Absent
Item
patients must not have progressed within 60 days of last therapy
boolean
C0242656 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Allogeneic hematopoietic stem cell transplant Absent
Item
not received allogeneic stem cell transplant
boolean
C4255274 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Standard therapy Options Lacking
Item
no reasonable standard therapeutic options available
boolean
C2936643 (UMLS CUI [1,1])
C1518601 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Glucose-6-phosphate dehydrogenase normal
Item
glucose 6 phosphate dehydrogenase status normal
boolean
C1167968 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Serum creatinine normal | Transaminases Normal
Item
normal creatinine and transaminase
boolean
C0438244 (UMLS CUI [1])
C0002594 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
Childbearing Potential Pregnancy test negative
Item
women of child-bearing potential confirm negative pregnancy test
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Comorbidity Significant
Item
significant co-morbid disorders
boolean
C0009488 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Psychiatric symptom Significant
Item
significant psychiatric symptoms
boolean
C0233401 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Tobacco use
Item
smoking
boolean
C0543414 (UMLS CUI [1])
Alcohol intake above recommended sensible limits | Drug use Excessive
Item
excessive alcohol or drug use
boolean
C0560219 (UMLS CUI [1])
C2239127 (UMLS CUI [2,1])
C0442802 (UMLS CUI [2,2])
Study Subject Participation Status | Therapy, Investigational
Item
enrollment in other experimental therapy
boolean
C2348568 (UMLS CUI [1])
C0949266 (UMLS CUI [2])
Communicable Disease
Item
active infection
boolean
C0009450 (UMLS CUI [1])
Disease Response | Therapeutic procedure Recent
Item
patients experiencing ongoing response to recent treatments
boolean
C1704632 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
Chemotherapy | Biological treatment
Item
patients who have received chemotherapy within 30 days or biological therapy within 6 weeks
boolean
C0392920 (UMLS CUI [1])
C1531518 (UMLS CUI [2])

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