Eligibility Hypertension NCT01709136

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
recipients of primary liver (cadaver/liver, whole/segmental) transplants 5- 30 years old.
Beschrijving

Recipient Transplanted liver Primary | Transplant from cadaver Whole | Transplant from cadaver Segmental | Age

Datatype

boolean

Alias
UMLS CUI [1,1]
C1709854
UMLS CUI [1,2]
C1280833
UMLS CUI [1,3]
C0205225
UMLS CUI [2,1]
C1456051
UMLS CUI [2,2]
C0444667
UMLS CUI [3,1]
C1456051
UMLS CUI [3,2]
C0205122
UMLS CUI [4]
C0001779
rejection-free post-transplant course for at least 3 months
Beschrijving

Liver transplant rejection Free of Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0400968
UMLS CUI [1,2]
C0332296
UMLS CUI [1,3]
C0449238
renal dysfunction (15% decrease in age-adjusted calculated creatinine clearance)
Beschrijving

Renal dysfunction | Creatinine clearance estimation decreased Age adjusted

Datatype

boolean

Alias
UMLS CUI [1]
C3279454
UMLS CUI [2,1]
C1262229
UMLS CUI [2,2]
C0001779
UMLS CUI [2,3]
C0456081
hypertension requiring anti-hypertensive mediations.
Beschrijving

Hypertensive disease Requirement Antihypertensive Agents

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0003364
informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
weight ≥15 kg.
Beschrijving

Body Weight

Datatype

boolean

Alias
UMLS CUI [1]
C0005910
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
rejection or infections within 3 months of enrollment.
Beschrijving

Rejection | Infection

Datatype

boolean

Alias
UMLS CUI [1]
C0018129
UMLS CUI [2]
C3714514
intent to continue tac
Beschrijving

Tacrolimus Continue Intent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085149
UMLS CUI [1,2]
C0549178
UMLS CUI [1,3]
C1283828
active participation in ongoing studies of immunosuppressive agents.
Beschrijving

Study Subject Participation Status | Immunosuppressive Agents

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0021081
lack of informed consent.
Beschrijving

Informed Consent Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
pregnant or breast feeding
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
hiv positive
Beschrijving

HIV Seropositivity

Datatype

boolean

Alias
UMLS CUI [1]
C0019699

Similar models

Eligibility Hypertension NCT01709136

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Recipient Transplanted liver Primary | Transplant from cadaver Whole | Transplant from cadaver Segmental | Age
Item
recipients of primary liver (cadaver/liver, whole/segmental) transplants 5- 30 years old.
boolean
C1709854 (UMLS CUI [1,1])
C1280833 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C1456051 (UMLS CUI [2,1])
C0444667 (UMLS CUI [2,2])
C1456051 (UMLS CUI [3,1])
C0205122 (UMLS CUI [3,2])
C0001779 (UMLS CUI [4])
Liver transplant rejection Free of Duration
Item
rejection-free post-transplant course for at least 3 months
boolean
C0400968 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Renal dysfunction | Creatinine clearance estimation decreased Age adjusted
Item
renal dysfunction (15% decrease in age-adjusted calculated creatinine clearance)
boolean
C3279454 (UMLS CUI [1])
C1262229 (UMLS CUI [2,1])
C0001779 (UMLS CUI [2,2])
C0456081 (UMLS CUI [2,3])
Hypertensive disease Requirement Antihypertensive Agents
Item
hypertension requiring anti-hypertensive mediations.
boolean
C0020538 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0003364 (UMLS CUI [1,3])
Informed Consent
Item
informed consent.
boolean
C0021430 (UMLS CUI [1])
Body Weight
Item
weight ≥15 kg.
boolean
C0005910 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Rejection | Infection
Item
rejection or infections within 3 months of enrollment.
boolean
C0018129 (UMLS CUI [1])
C3714514 (UMLS CUI [2])
Tacrolimus Continue Intent
Item
intent to continue tac
boolean
C0085149 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,3])
Study Subject Participation Status | Immunosuppressive Agents
Item
active participation in ongoing studies of immunosuppressive agents.
boolean
C2348568 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
Informed Consent Lacking
Item
lack of informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
HIV Seropositivity
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])