Informações:
Falhas:
ID
33515
Descrição
Effect of An Oral Absorbent AST-120 in Late-stage Chronic Kidney Disease (CKD) Patients.; ODM derived from: https://clinicaltrials.gov/show/NCT01681303
Link
https://clinicaltrials.gov/show/NCT01681303
Palavras-chave
Versões (1)
- 11/12/2018 11/12/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
11 de dezembro de 2018
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 Chronic Kidney Disease NCT01681303
Eligibility Chronic Kidney Disease NCT01681303
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Kidney Disease NCT01681303
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Adult | Age
Item
adults aged > 18 year-old or < 85 year-old
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Estimated Glomerular Filtration Rate | Creatinine clearance rate
Item
egfr or ccr < 60 ml/min
boolean
C3811844 (UMLS CUI [1])
C0546737 (UMLS CUI [2])
C0546737 (UMLS CUI [2])
Hemoglobin measurement | Erythropoiesis-stimulating Agent Absent | Iron Storage | Serum ferritin measurement | Transferrin saturation measurement
Item
hemoglobin < 10 g/dl, esa-naïve, had adequate iron storage (serum ferritin > 200 ng/dl and transferrin saturation > 20%)
boolean
C0518015 (UMLS CUI [1])
C2917382 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0302583 (UMLS CUI [3,1])
C1698986 (UMLS CUI [3,2])
C0696113 (UMLS CUI [4])
C1277709 (UMLS CUI [5])
C2917382 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0302583 (UMLS CUI [3,1])
C1698986 (UMLS CUI [3,2])
C0696113 (UMLS CUI [4])
C1277709 (UMLS CUI [5])
Absence Improvement Renal Spontaneous | Disease Progression Renal Absent
Item
no spontaneous renal improvement or progression in past 3 months.
boolean
C0332197 (UMLS CUI [1,1])
C2986411 (UMLS CUI [1,2])
C0022646 (UMLS CUI [1,3])
C0205359 (UMLS CUI [1,4])
C0242656 (UMLS CUI [2,1])
C0022646 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C2986411 (UMLS CUI [1,2])
C0022646 (UMLS CUI [1,3])
C0205359 (UMLS CUI [1,4])
C0242656 (UMLS CUI [2,1])
C0022646 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Kidney Transplantation | Liver Cirrhosis | Bone Marrow Disease
Item
renal transplant recipients, liver cirrhosis, bone marrow disorder
boolean
C0022671 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
C0005956 (UMLS CUI [3])
C0023890 (UMLS CUI [2])
C0005956 (UMLS CUI [3])
Blood pressure determination Occurrence Quantity
Item
blood pressure > 170/80 mmhg in 3 occasions
boolean
C0005824 (UMLS CUI [1,1])
C2745955 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C2745955 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Cardiovascular Disease | Coronary Artery Disease | Myocardial Ischemia | Cerebrovascular Disorders | Peripheral Arterial Diseases | Gastrointestinal Hemorrhage
Item
recent cardiovascular disease (coronary artery disease, myocardial ischemia, cerebrovascular disease or peripheral artery disease) or gastrointestinal bleeding in past 3 months
boolean
C0007222 (UMLS CUI [1])
C1956346 (UMLS CUI [2])
C0151744 (UMLS CUI [3])
C0007820 (UMLS CUI [4])
C1704436 (UMLS CUI [5])
C0017181 (UMLS CUI [6])
C1956346 (UMLS CUI [2])
C0151744 (UMLS CUI [3])
C0007820 (UMLS CUI [4])
C1704436 (UMLS CUI [5])
C0017181 (UMLS CUI [6])
Tubular necrosis
Item
acute tubular necrosis in the past 3 months
boolean
C1720775 (UMLS CUI [1])
Study Subject Participation Status Unwilling
Item
unwilling to participate in the trial
boolean
C2348568 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,2])