Informações:
Falhas:
ID
42966
Descrição
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
Palavras-chave
Versões (2)
- 10/04/2017 10/04/2017 -
- 17/09/2021 17/09/2021 -
Transferido a
17 de setembro de 2021
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Hypertension NCT01709136
Eligibility Hypertension NCT01709136
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01709136
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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])
C0439751 (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])
C0439751 (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])