ID

39170

Beschrijving

Chinese Medicine on Deferring Dialysis Initiation; ODM derived from: https://clinicaltrials.gov/show/NCT02194946

Link

https://clinicaltrials.gov/show/NCT02194946

Trefwoorden

Versies (1)
  1. 07-12-19 07-12-19 -
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See clinicaltrials.gov

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7 december 2019

DOI

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Creative Commons BY 4.0
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Eligibility End-Stage Renal Disease NCT02194946

Engels

Eligibility End-Stage Renal Disease NCT02194946

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18-75 years;
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
egfr ＜15 ml/min per 1.73 m2;
Beschrijving

Estimated Glomerular Filtration Rate

Datatype

boolean

Alias
UMLS CUI [1]
C3811844
non-diabetic ckd, which should be identified by biopsy or patients' medical histories.
Beschrijving

Chronic Kidney Disease Biopsy | Chronic Kidney Disease Medical History | Diabetes Mellitus Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C0005558
UMLS CUI [2,1]
C1561643
UMLS CUI [2,2]
C0262926
UMLS CUI [3,1]
C0011849
UMLS CUI [3,2]
C0332197
yellow race.
Beschrijving

Racial group Yellow

Datatype

boolean

Alias
UMLS CUI [1,1]
C0034510
UMLS CUI [1,2]
C0221205
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
clinical indications of dialysis still occur after conservative kidney management for 1 week, which will be ruled out as hemoglobin < 70g/l; or serum potassium> 5.5mmol/l; or co2cp <13mmol/l; or epi-gfr≤5ml/min/1.73m2 ;
Beschrijving

Indication Dialysis | Status post Conservative Treatment Kidney | Hemoglobin measurement | Serum potassium measurement | Carbon dioxide combining power measurement | Glomerular Filtration Rate CKD-EPI

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0011946
UMLS CUI [2,1]
C0231290
UMLS CUI [2,2]
C0459914
UMLS CUI [2,3]
C0022646
UMLS CUI [3]
C0518015
UMLS CUI [4]
C0302353
UMLS CUI [5]
C0546630
UMLS CUI [6,1]
C0017654
UMLS CUI [6,2]
C2964649
pregnant or lactating.
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
critical status, such as alimentary tract hemorrhage or decompensated cirrhosis;
Beschrijving

Patient status determination, critical | Gastrointestinal Hemorrhage | Decompensated cirrhosis of liver

Datatype

boolean

Alias
UMLS CUI [1]
C0184770
UMLS CUI [2]
C0017181
UMLS CUI [3]
C1619727
history of malignancy other than a successfully and completely treated carcinoma;
Beschrijving

Malignant Neoplasms | Exception Carcinoma Treated Completely

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007097
UMLS CUI [2,3]
C1522326
UMLS CUI [2,4]
C0205197
any condition (mental or physical) that would interfere with the patient's ability to comply with the study protocol;
Beschrijving

Mental condition Interferes with Protocol Compliance | Individual Physical Condition Interferes with Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1,1]
C3840291
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0525058
UMLS CUI [2,1]
C3714565
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0525058
concurrent or current treatment with glucocorticoid or immunosuppressant agents in last 3 months;
Beschrijving

Glucocorticoids | Immunosuppressive Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0017710
UMLS CUI [2]
C0021081
participation in any other clinical trial;
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
known or suspected allergy to certain agents involved;
Beschrijving

Hypersensitivity Investigational New Drugs | Hypersensitivity Suspected Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0750491
UMLS CUI [2,3]
C0013230
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Similar models

Eligibility End-Stage Renal Disease NCT02194946

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 18-75 years;
boolean
C0001779 (UMLS CUI [1])
Estimated Glomerular Filtration Rate
Item
egfr ＜15 ml/min per 1.73 m2;
boolean
C3811844 (UMLS CUI [1])
Chronic Kidney Disease Biopsy | Chronic Kidney Disease Medical History | Diabetes Mellitus Absent
Item
non-diabetic ckd, which should be identified by biopsy or patients' medical histories.
boolean
C1561643 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C1561643 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
C0011849 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Racial group Yellow
Item
yellow race.
boolean
C0034510 (UMLS CUI [1,1])
C0221205 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Indication Dialysis | Status post Conservative Treatment Kidney | Hemoglobin measurement | Serum potassium measurement | Carbon dioxide combining power measurement | Glomerular Filtration Rate CKD-EPI
Item
clinical indications of dialysis still occur after conservative kidney management for 1 week, which will be ruled out as hemoglobin < 70g/l; or serum potassium> 5.5mmol/l; or co2cp <13mmol/l; or epi-gfr≤5ml/min/1.73m2 ;
boolean
C3146298 (UMLS CUI [1,1])
C0011946 (UMLS CUI [1,2])
C0231290 (UMLS CUI [2,1])
C0459914 (UMLS CUI [2,2])
C0022646 (UMLS CUI [2,3])
C0518015 (UMLS CUI [3])
C0302353 (UMLS CUI [4])
C0546630 (UMLS CUI [5])
C0017654 (UMLS CUI [6,1])
C2964649 (UMLS CUI [6,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Patient status determination, critical | Gastrointestinal Hemorrhage | Decompensated cirrhosis of liver
Item
critical status, such as alimentary tract hemorrhage or decompensated cirrhosis;
boolean
C0184770 (UMLS CUI [1])
C0017181 (UMLS CUI [2])
C1619727 (UMLS CUI [3])
Malignant Neoplasms | Exception Carcinoma Treated Completely
Item
history of malignancy other than a successfully and completely treated carcinoma;
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007097 (UMLS CUI [2,2])
C1522326 (UMLS CUI [2,3])
C0205197 (UMLS CUI [2,4])
Mental condition Interferes with Protocol Compliance | Individual Physical Condition Interferes with Protocol Compliance
Item
any condition (mental or physical) that would interfere with the patient's ability to comply with the study protocol;
boolean
C3840291 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C3714565 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
Glucocorticoids | Immunosuppressive Agents
Item
concurrent or current treatment with glucocorticoid or immunosuppressant agents in last 3 months;
boolean
C0017710 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in any other clinical trial;
boolean
C2348568 (UMLS CUI [1])
Hypersensitivity Investigational New Drugs | Hypersensitivity Suspected Investigational New Drugs
Item
known or suspected allergy to certain agents involved;
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0013230 (UMLS CUI [2,3])
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