ID

20508

Description

Sodium Bicarbonate in Preventing Contrast Induced Nephropathy; ODM derived from: https://clinicaltrials.gov/show/NCT00531765

Link

https://clinicaltrials.gov/show/NCT00531765

Keywords

Versions (1)
  1. 2/28/17 2/28/17 -
Uploaded on

February 28, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Contrast Induced Nephropathy NCT00531765

English

Eligibility Contrast Induced Nephropathy NCT00531765

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
current or previous breast cancer
Description

Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0678222
current or previous prostate cancer
Description

Prostate carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0600139
raised prostate specific antigen or abnormal per rectal examination unless prostate cancer excluded after specialist urology opinion
Description

Raised prostate specific antigen | Prostate specific antigen abnormal Rectal examination | Prostate carcinoma Exclusion

Data type

boolean

Alias
UMLS CUI [1]
C0178415
UMLS CUI [2,1]
C0580555
UMLS CUI [2,2]
C0199900
UMLS CUI [3,1]
C0600139
UMLS CUI [3,2]
C2828389
severe symptoms of benign prostatic hypertrophy ('prostatism')
Description

Benign prostatic hypertrophy Symptom severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0005001
UMLS CUI [1,2]
C0436345
treatment with testosterone in the 3 months prior to the trial
Description

Testosterone

Data type

boolean

Alias
UMLS CUI [1]
C0039601
investigational drug treatment in the 3 months prior to the trial
Description

Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C0013230
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Similar models

Eligibility Contrast Induced Nephropathy NCT00531765

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Item Group
C0680251 (UMLS CUI)
Breast Carcinoma
Item
current or previous breast cancer
boolean
C0678222 (UMLS CUI [1])
Prostate carcinoma
Item
current or previous prostate cancer
boolean
C0600139 (UMLS CUI [1])
Raised prostate specific antigen | Prostate specific antigen abnormal Rectal examination | Prostate carcinoma Exclusion
Item
raised prostate specific antigen or abnormal per rectal examination unless prostate cancer excluded after specialist urology opinion
boolean
C0178415 (UMLS CUI [1])
C0580555 (UMLS CUI [2,1])
C0199900 (UMLS CUI [2,2])
C0600139 (UMLS CUI [3,1])
C2828389 (UMLS CUI [3,2])
Benign prostatic hypertrophy Symptom severe
Item
severe symptoms of benign prostatic hypertrophy ('prostatism')
boolean
C0005001 (UMLS CUI [1,1])
C0436345 (UMLS CUI [1,2])
Testosterone
Item
treatment with testosterone in the 3 months prior to the trial
boolean
C0039601 (UMLS CUI [1])
Investigational New Drugs
Item
investigational drug treatment in the 3 months prior to the trial
boolean
C0013230 (UMLS CUI [1])
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