ID

20070

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00395005

Nyckelord

Versioner (1)
  1. 2017-02-05 2017-02-05 -
Uppladdad den

5 februari 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Chronic Kidney Disease NCT00395005

Engelsk

Eligibility Chronic Kidney Disease NCT00395005

1 Formulär  
Inclusion Criteria
Beskrivning

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.
Beskrivning

Study Subject Participation Status | Informed Consent

Datatyp

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.
Beskrivning

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

Datatyp

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
Beskrivning

Urine protein/creatinine ratio measurement Random Initial

Datatyp

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of allergy to pentoxifylline;
Beskrivning

Pentoxifylline allergy

Datatyp

boolean

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

Breast Feeding | Pregnancy

Datatyp

boolean

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

Urinary tract obstruction

Datatyp

boolean

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

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

Datatyp

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);
Beskrivning

Congestive heart failure New York Heart Association Classification

Datatyp

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;
Beskrivning

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

Datatyp

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;
Beskrivning

Cerebral Hemorrhage

Datatyp

boolean

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

Retinal Hemorrhage

Datatyp

boolean

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

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

Datatyp

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;
Beskrivning

Uncontrolled hypertension Severe | Systolic Pressure | Diastolic blood pressure

Datatyp

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;
Beskrivning

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

Datatyp

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);
Beskrivning

Biliary obstruction | Cholestasis

Datatyp

boolean

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

Malignant Neoplasm

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
Tillbaka till toppen

Similar models

Eligibility Chronic Kidney Disease NCT00395005

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial