Informações:
Falhas:
ID
29299
Descrição
Sympathetic Activity in Patients With End-stage Renal Disease on Peritoneal Dialysis; ODM derived from: https://clinicaltrials.gov/show/NCT01228279
Link
https://clinicaltrials.gov/show/NCT01228279
Palavras-chave
Versões (1)
- 17/03/2018 17/03/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
17 de março de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility End-stage Renal Disease (ESRD) NCT01228279
Eligibility End-stage Renal Disease (ESRD) NCT01228279
- StudyEvent: Eligibility
Similar models
Eligibility End-stage Renal Disease (ESRD) NCT01228279
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Adult | Age
Item
adult (age 18 years and older)
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Kidney Failure, Chronic | Chronic Kidney Disease Stage
Item
patients with end-stage renal disease(esrd)/chronic kidney disease(ckd)stage 5
boolean
C0022661 (UMLS CUI [1])
C1561643 (UMLS CUI [2,1])
C2074731 (UMLS CUI [2,2])
C1561643 (UMLS CUI [2,1])
C2074731 (UMLS CUI [2,2])
Diabetes Mellitus
Item
diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Acute Coronary Syndrome
Item
acute coronary syndrome in the past 6 months
boolean
C0948089 (UMLS CUI [1])
Cardiac Arrhythmia | Second degree atrioventricular block | Complete atrioventricular block | Premature ventricular complexes Classification
Item
cardiac arrhythmias (2nd and 3rd degree heart block or premature ventricular complexes in lown classes 4 or 5)
boolean
C0003811 (UMLS CUI [1])
C0264906 (UMLS CUI [2])
C0151517 (UMLS CUI [3])
C0151636 (UMLS CUI [4,1])
C0008902 (UMLS CUI [4,2])
C0264906 (UMLS CUI [2])
C0151517 (UMLS CUI [3])
C0151636 (UMLS CUI [4,1])
C0008902 (UMLS CUI [4,2])
Symptoms Suggestive of Obstructive Sleep Apnea Epworth Sleepiness Scale | Symptoms Suggestive of Central Sleep Apnea Epworth Sleepiness Scale
Item
symptoms suggestive of obstructive or central sleep apnea (with a score of > 10 on epworth sleepiness scale)
boolean
C1457887 (UMLS CUI [1,1])
C0332299 (UMLS CUI [1,2])
C0520679 (UMLS CUI [1,3])
C3541276 (UMLS CUI [1,4])
C1457887 (UMLS CUI [2,1])
C0332299 (UMLS CUI [2,2])
C0520680 (UMLS CUI [2,3])
C3541276 (UMLS CUI [2,4])
C0332299 (UMLS CUI [1,2])
C0520679 (UMLS CUI [1,3])
C3541276 (UMLS CUI [1,4])
C1457887 (UMLS CUI [2,1])
C0332299 (UMLS CUI [2,2])
C0520680 (UMLS CUI [2,3])
C3541276 (UMLS CUI [2,4])
Clonidine
Item
patients taking clonidine
boolean
C0009014 (UMLS CUI [1])
Body mass index
Item
body mass index (bmi) > 34
boolean
C1305855 (UMLS CUI [1])
Informed Consent Unable
Item
patients unable to give consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Leg Injury Involving Nerve damage
Item
patients with leg injury involving nerve damage
boolean
C0023220 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C0161479 (UMLS CUI [1,3])
C1314939 (UMLS CUI [1,2])
C0161479 (UMLS CUI [1,3])
Anticoagulants
Item
patients taking anticoagulant medication
boolean
C0003280 (UMLS CUI [1])
Blood Coagulation Disorder | Liver disease
Item
patients with significant bleeding disorder or liver disorder
boolean
C0005779 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0023895 (UMLS CUI [2])
Hemoglobin measurement
Item
hemoglobin <1.05 g/dl at the time of initiation of therapy
boolean
C0518015 (UMLS CUI [1])
Unilateral nephrectomy | Bilateral total nephrectomy
Item
patients with unilateral or bilateral nephrectomy
boolean
C0194083 (UMLS CUI [1])
C0194084 (UMLS CUI [2])
C0194084 (UMLS CUI [2])
Kidney Transplantation Planned
Item
planned kidney transplant in the next 4 months
boolean
C0022671 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy under 6 months
boolean
C0023671 (UMLS CUI [1])
Oliguria
Item
oliguria (urine output less than 400 ml per day)
boolean
C0028961 (UMLS CUI [1])