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ID
21104
Description
Pharmacokinectics of Sirolimus and Tacrolimus in Liver Transplant Recipients With Tacrolimus Toxicity; ODM derived from: https://clinicaltrials.gov/show/NCT01709136
Link
https://clinicaltrials.gov/show/NCT01709136
Keywords
Versions (2)
- 4/10/17 4/10/17 -
- 9/17/21 9/17/21 -
Uploaded on
April 10, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Hypertension NCT01709136
Eligibility Hypertension NCT01709136
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01709136
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
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])
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])
Rejection | Infection
Item
rejection or infections within 3 months of enrollment.
boolean
C0018129 (UMLS CUI [1])
C3714514 (UMLS CUI [2])
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])
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])
C0021081 (UMLS CUI [2])
Informed Consent Lacking
Item
lack of informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
HIV Seropositivity
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])