ID

20070

Beschrijving

Correlation of Urinary Kallikrein With Cytokines, Proteinuria and Renal Function in Chronic Renal Disease Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00395005

Link

https://clinicaltrials.gov/show/NCT00395005

Trefwoorden

Versies (1)
  1. 05-02-17 05-02-17 -
Geüploaded op

5 februari 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Chronic Kidney Disease NCT00395005

Engels

Eligibility Chronic Kidney Disease NCT00395005

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
during june 2004 and june 2005 who participate the clinical study "efficacy of pentoxifylline on chronic kidney disease" (clinicaltrials.gov identifier: nct00155246)and sign the informed consent.
Beschrijving

Study Subject Participation Status | Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0021430
chronic kidney disease history > 3 months, serum creatinine: 1.1~6.0 mg/dl in female. 1.3~6.2 mg/dl in male.
Beschrijving

Chronic kidney disease Disease length | Creatinine measurement, serum | Gender

Datatype

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C0872146
UMLS CUI [2]
C0201976
UMLS CUI [3]
C0079399
initial random urine protein (mg/dl) /creatinine (mg/dl) ratio > 0.5
Beschrijving

Urine protein/creatinine ratio measurement Random Initial

Datatype

boolean

Alias
UMLS CUI [1,1]
C1096054
UMLS CUI [1,2]
C0439605
UMLS CUI [1,3]
C0205265
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of allergy to pentoxifylline;
Beschrijving

Pentoxifylline allergy

Datatype

boolean

Alias
UMLS CUI [1]
C0571995
females are nursing or pregnant;
Beschrijving

Breast Feeding | Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006147
UMLS CUI [2]
C0032961
obstructive uropathy;
Beschrijving

Urinary tract obstruction

Datatype

boolean

Alias
UMLS CUI [1]
C0178879
unable to stop chronic immunosuppressive therapy, nsaid;
Beschrijving

Therapeutic immunosuppression chronic Stop Unable | Anti-Inflammatory Agents, Non-Steroidal

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021079
UMLS CUI [1,2]
C0205191
UMLS CUI [1,3]
C1947925
UMLS CUI [1,4]
C1299582
UMLS CUI [2]
C0003211
congestive heart failure (new york heart association functional class iii or iv);
Beschrijving

Congestive heart failure New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1275491
unstable angina, myocardial infarction, coronary artery bypass graft surgery, percutaneous coronary intervention, within the past 6 months prior to signing the informed consent form;
Beschrijving

Angina, Unstable | Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0027051
UMLS CUI [3]
C0010055
UMLS CUI [4]
C1532338
cerebral hemorrhage within the past 6 months prior to signing the informed consent form;
Beschrijving

Cerebral Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C2937358
retinal hemorrhage within the past 6 months prior to signing the informed consent form;
Beschrijving

Retinal Hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0035317
known or suspected secondary hypertension (e.g., primary aldosteronism, renovascular hypertension, pheochromocytoma);
Beschrijving

Secondary hypertension | Secondary hypertension Suspected | Conn Syndrome | Hypertension, Renovascular | Pheochromocytoma

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2,1]
C0155616
UMLS CUI [2,2]
C0750491
UMLS CUI [3]
C1384514
UMLS CUI [4]
C0020545
UMLS CUI [5]
C0031511
severe uncontrolled hypertension with sbp > 220 mmhg and/or dbp > 115 mmhg;
Beschrijving

Uncontrolled hypertension Severe | Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1,1]
C1868885
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
hepatic dysfunction as defined by the following laboratory parameters: alt or ast > 2 times the upper limit of the normal range;
Beschrijving

Liver Dysfunction Laboratory Results | Alanine aminotransferase increased | Aspartate aminotransferase increased

Datatype

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C1254595
UMLS CUI [2]
C0151905
UMLS CUI [3]
C0151904
biliary obstructive disorders (e.g. cholestasis);
Beschrijving

Biliary obstruction | Cholestasis

Datatype

boolean

Alias
UMLS CUI [1]
C0400979
UMLS CUI [2]
C0008370
active malignancy
Beschrijving

Malignant Neoplasm

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
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Similar models

Eligibility Chronic Kidney Disease NCT00395005

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Study Subject Participation Status | Informed Consent
Item
during june 2004 and june 2005 who participate the clinical study "efficacy of pentoxifylline on chronic kidney disease" (clinicaltrials.gov identifier: nct00155246)and sign the informed consent.
boolean
C2348568 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
Chronic kidney disease Disease length | Creatinine measurement, serum | Gender
Item
chronic kidney disease history > 3 months, serum creatinine: 1.1~6.0 mg/dl in female. 1.3~6.2 mg/dl in male.
boolean
C1561643 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0201976 (UMLS CUI [2])
C0079399 (UMLS CUI [3])
Urine protein/creatinine ratio measurement Random Initial
Item
initial random urine protein (mg/dl) /creatinine (mg/dl) ratio > 0.5
boolean
C1096054 (UMLS CUI [1,1])
C0439605 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Pentoxifylline allergy
Item
history of allergy to pentoxifylline;
boolean
C0571995 (UMLS CUI [1])
Breast Feeding | Pregnancy
Item
females are nursing or pregnant;
boolean
C0006147 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
Urinary tract obstruction
Item
obstructive uropathy;
boolean
C0178879 (UMLS CUI [1])
Therapeutic immunosuppression chronic Stop Unable | Anti-Inflammatory Agents, Non-Steroidal
Item
unable to stop chronic immunosuppressive therapy, nsaid;
boolean
C0021079 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C1947925 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,4])
C0003211 (UMLS CUI [2])
Congestive heart failure New York Heart Association Classification
Item
congestive heart failure (new york heart association functional class iii or iv);
boolean
C0018802 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Angina, Unstable | Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
unstable angina, myocardial infarction, coronary artery bypass graft surgery, percutaneous coronary intervention, within the past 6 months prior to signing the informed consent form;
boolean
C0002965 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
C1532338 (UMLS CUI [4])
Cerebral Hemorrhage
Item
cerebral hemorrhage within the past 6 months prior to signing the informed consent form;
boolean
C2937358 (UMLS CUI [1])
Retinal Hemorrhage
Item
retinal hemorrhage within the past 6 months prior to signing the informed consent form;
boolean
C0035317 (UMLS CUI [1])
Secondary hypertension | Secondary hypertension Suspected | Conn Syndrome | Hypertension, Renovascular | Pheochromocytoma
Item
known or suspected secondary hypertension (e.g., primary aldosteronism, renovascular hypertension, pheochromocytoma);
boolean
C0155616 (UMLS CUI [1])
C0155616 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C1384514 (UMLS CUI [3])
C0020545 (UMLS CUI [4])
C0031511 (UMLS CUI [5])
Uncontrolled hypertension Severe | Systolic Pressure | Diastolic blood pressure
Item
severe uncontrolled hypertension with sbp > 220 mmhg and/or dbp > 115 mmhg;
boolean
C1868885 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Liver Dysfunction Laboratory Results | Alanine aminotransferase increased | Aspartate aminotransferase increased
Item
hepatic dysfunction as defined by the following laboratory parameters: alt or ast > 2 times the upper limit of the normal range;
boolean
C0086565 (UMLS CUI [1,1])
C1254595 (UMLS CUI [1,2])
C0151905 (UMLS CUI [2])
C0151904 (UMLS CUI [3])
Biliary obstruction | Cholestasis
Item
biliary obstructive disorders (e.g. cholestasis);
boolean
C0400979 (UMLS CUI [1])
C0008370 (UMLS CUI [2])
Malignant Neoplasm
Item
active malignancy
boolean
C0006826 (UMLS CUI [1])
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