ID

16874

Description

Trial to Assess Chelation Therapy (TACT); ODM derived from: https://clinicaltrials.gov/show/NCT00044213

Link

https://clinicaltrials.gov/show/NCT00044213

Keywords

Versions (1)
  1. 8/11/16 8/11/16 -
Uploaded on

August 11, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00044213

English

Eligibility Coronary Artery Disease NCT00044213

1 forms  
Criteria
Description

Criteria

heart attack at least 6 weeks prior to study start
Description

Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1]
C0027051
exclusion criteria for participants:
Description

Exclusion Criteria

Data type

boolean

Alias
UMLS CUI [1]
C0680251
serum creatinie level greater than 2.0 mg/dl
Description

Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0201976
platelet count less than 100,000/µl
Description

Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1]
C0032181
blood pressure greater than 160/100
Description

Blood Pressure

Data type

boolean

Alias
UMLS CUI [1]
C0005823
chelation therapy within 5 years prior to study start
Description

Chelation Therapy

Data type

boolean

Alias
UMLS CUI [1]
C0007975
history of allergic reactions to edta or any of the therapy's components
Description

Allergic Reaction EDTA | Allergic Reaction Therapeutic procedure Component

Data type

boolean

Alias
UMLS CUI [1,1]
C1527304
UMLS CUI [1,2]
C0013618
UMLS CUI [2,1]
C1527304
UMLS CUI [2,2]
C0087111
UMLS CUI [2,3]
C1705248
coronary or carotid revascularization procedures within 6 months prior to study start or a scheduled revascularization
Description

Coronary revascularisation | Carotid revascularisation | Revascularization Planned

Data type

boolean

Alias
UMLS CUI [1]
C0877341
UMLS CUI [2]
C3495793
UMLS CUI [3,1]
C0581603
UMLS CUI [3,2]
C1301732
cigarette smoking within 3 months prior to study start
Description

Cigarette smoking

Data type

boolean

Alias
UMLS CUI [1]
C0700219
childbearing potential
Description

Childbearing Potential

Data type

boolean

Alias
UMLS CUI [1]
C3831118
history of liver disease
Description

Liver disease

Data type

boolean

Alias
UMLS CUI [1]
C0023895
active heart failure or heart failure hospitalization within 6 months.
Description

Heart failure | Hospitalization Heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2,1]
C0019993
UMLS CUI [2,2]
C0018801
diagnoses of additional medical conditions that could otherwise limit patient survival
Description

Comorbidity Limiting Survival Patient

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0038952
UMLS CUI [1,4]
C0030705
inability to tolerate 500-ml infusions weekly.
Description

Infusion Quantity Tolerance Limited

Data type

boolean

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0231197
UMLS CUI [1,4]
C0439801
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Similar models

Eligibility Coronary Artery Disease NCT00044213

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Myocardial Infarction
Item
heart attack at least 6 weeks prior to study start
boolean
C0027051 (UMLS CUI [1])
Exclusion Criteria
Item
exclusion criteria for participants:
boolean
C0680251 (UMLS CUI [1])
Creatinine measurement, serum
Item
serum creatinie level greater than 2.0 mg/dl
boolean
C0201976 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count less than 100,000/µl
boolean
C0032181 (UMLS CUI [1])
Blood Pressure
Item
blood pressure greater than 160/100
boolean
C0005823 (UMLS CUI [1])
Chelation Therapy
Item
chelation therapy within 5 years prior to study start
boolean
C0007975 (UMLS CUI [1])
Allergic Reaction EDTA | Allergic Reaction Therapeutic procedure Component
Item
history of allergic reactions to edta or any of the therapy's components
boolean
C1527304 (UMLS CUI [1,1])
C0013618 (UMLS CUI [1,2])
C1527304 (UMLS CUI [2,1])
C0087111 (UMLS CUI [2,2])
C1705248 (UMLS CUI [2,3])
Coronary revascularisation | Carotid revascularisation | Revascularization Planned
Item
coronary or carotid revascularization procedures within 6 months prior to study start or a scheduled revascularization
boolean
C0877341 (UMLS CUI [1])
C3495793 (UMLS CUI [2])
C0581603 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
Cigarette smoking
Item
cigarette smoking within 3 months prior to study start
boolean
C0700219 (UMLS CUI [1])
Childbearing Potential
Item
childbearing potential
boolean
C3831118 (UMLS CUI [1])
Liver disease
Item
history of liver disease
boolean
C0023895 (UMLS CUI [1])
Heart failure | Hospitalization Heart failure
Item
active heart failure or heart failure hospitalization within 6 months.
boolean
C0018801 (UMLS CUI [1])
C0019993 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
Comorbidity Limiting Survival Patient
Item
diagnoses of additional medical conditions that could otherwise limit patient survival
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0038952 (UMLS CUI [1,3])
C0030705 (UMLS CUI [1,4])
Infusion Quantity Tolerance Limited
Item
inability to tolerate 500-ml infusions weekly.
boolean
C0574032 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0231197 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,4])
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