Informações:
Falhas:
ID
39513
Descrição
Aquaresis Utility for Hyponatremic Acute Heart Failure Study; ODM derived from: https://clinicaltrials.gov/show/NCT02183792
Link
https://clinicaltrials.gov/show/NCT02183792
Palavras-chave
Versões (1)
- 21/01/2020 21/01/2020 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
21 de janeiro de 2020
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Heart Failure NCT02183792
Eligibility Heart Failure NCT02183792
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT02183792
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Heart failure | Sign or Symptom Fluid overload | Raised jugular venous pressure | Rales | Edema
Item
acute hf with signs or symptoms of volume overload [i.e. elevated jugular venous pulsation (jvp), rales, edema]
boolean
C0018801 (UMLS CUI [1])
C3540840 (UMLS CUI [2,1])
C0546817 (UMLS CUI [2,2])
C0520861 (UMLS CUI [3])
C0034642 (UMLS CUI [4])
C0013604 (UMLS CUI [5])
C3540840 (UMLS CUI [2,1])
C0546817 (UMLS CUI [2,2])
C0520861 (UMLS CUI [3])
C0034642 (UMLS CUI [4])
C0013604 (UMLS CUI [5])
Serum sodium measurement
Item
serum sodium ≤ 130 meq/l at time of or within first 48 hours of hospitalization
boolean
C0523891 (UMLS CUI [1])
Subject is Randomized
Item
randomized within 48 hours of presentation to hospital
boolean
C3815594 (UMLS CUI [1])
Age
Item
≥ 18 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Hyponatremia Symptomatic Severe | Treatment required
Item
severe symptomatic hyponatremia requiring acute treatment
boolean
C0020625 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0332121 (UMLS CUI [2])
C0231220 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0332121 (UMLS CUI [2])
Renal Insufficiency Severe | On admission | Creatinine clearance measurement
Item
severe renal impairment upon admission (creatinine clearance < 20 ml/min)
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0457453 (UMLS CUI [2])
C0373595 (UMLS CUI [3])
C0205082 (UMLS CUI [1,2])
C0457453 (UMLS CUI [2])
C0373595 (UMLS CUI [3])
Renal Replacement Therapy Dependence | Requirement Admission
Item
renal replacement therapy dependent, or requiring upon admission
boolean
C0206074 (UMLS CUI [1,1])
C0439857 (UMLS CUI [1,2])
C1514873 (UMLS CUI [2,1])
C0809949 (UMLS CUI [2,2])
C0439857 (UMLS CUI [1,2])
C1514873 (UMLS CUI [2,1])
C0809949 (UMLS CUI [2,2])
Acute Coronary Syndrome On admission
Item
acute coronary syndrome on admission
boolean
C0948089 (UMLS CUI [1,1])
C0457453 (UMLS CUI [1,2])
C0457453 (UMLS CUI [1,2])
Shock, Cardiogenic | Requirement Vasoconstrictor Agents Intravenous
Item
evidence of cardiogenic shock or requiring intravenous vasopressors
boolean
C0036980 (UMLS CUI [1])
C1514873 (UMLS CUI [2,1])
C0042397 (UMLS CUI [2,2])
C1522726 (UMLS CUI [2,3])
C1514873 (UMLS CUI [2,1])
C0042397 (UMLS CUI [2,2])
C1522726 (UMLS CUI [2,3])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Requirement CYP3A4 Inhibitor Strong | Clarithromycin | Ketoconazole | Itraconazole | Ritonavir | Indinavir | Nelfinavir | Saquinavir | nefazodone | telithromycin
Item
patient requiring concomitant use of strong cyp3a4 inhibitors (clarithromycin, ketoconazole, itraconazole, ritonavir, indinavir, nelfinavir, saquinavir, nefazodone, and telithromycin)
boolean
C1514873 (UMLS CUI [1,1])
C3830624 (UMLS CUI [1,2])
C0442821 (UMLS CUI [1,3])
C0055856 (UMLS CUI [2])
C0022625 (UMLS CUI [3])
C0064113 (UMLS CUI [4])
C0292818 (UMLS CUI [5])
C0376637 (UMLS CUI [6])
C0525005 (UMLS CUI [7])
C0286738 (UMLS CUI [8])
C0068485 (UMLS CUI [9])
C0907410 (UMLS CUI [10])
C3830624 (UMLS CUI [1,2])
C0442821 (UMLS CUI [1,3])
C0055856 (UMLS CUI [2])
C0022625 (UMLS CUI [3])
C0064113 (UMLS CUI [4])
C0292818 (UMLS CUI [5])
C0376637 (UMLS CUI [6])
C0525005 (UMLS CUI [7])
C0286738 (UMLS CUI [8])
C0068485 (UMLS CUI [9])
C0907410 (UMLS CUI [10])