ID

20482

Descripción

Reduced Anti-Platelet Therapy With Pimecrolimus Drug Eluting Stent (RAPID); ODM derived from: https://clinicaltrials.gov/show/NCT00322543

Link

https://clinicaltrials.gov/show/NCT00322543

Palabras clave

  1. 25/2/17 25/2/17 -
Subido en

25 de febrero de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Coronary Disease NCT00322543

Eligibility Coronary Disease NCT00322543

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
general inclusion criteria
Descripción

Inclusion criteria General

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0205246
1. eligible for percutaneous coronary intervention (pci).
Descripción

Eligibility Percutaneous Coronary Intervention

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0680253
UMLS CUI [1,2]
C1532338
2. documented stable or unstable angina pectoris
Descripción

Stable angina | Angina, Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0340288
UMLS CUI [2]
C0002965
3. left ventricular ejection fraction (lvef) ≥25%
Descripción

Left ventricular ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
4. acceptable candidate for coronary artery bypass graft surgery (cabg).
Descripción

Indication Coronary Artery Bypass Surgery

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0010055
5. target lesion < 25 mm in length with rvd of 2.5 to 3.5 mm with visually estimated stenosis of >= 50 and < 100 %.
Descripción

Target Lesion Length | Reference Vessel Diameter | Stenosis Percentage

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C1444754
UMLS CUI [2,1]
C1706462
UMLS CUI [2,2]
C0005847
UMLS CUI [2,3]
C1301886
UMLS CUI [3,1]
C1261287
UMLS CUI [3,2]
C0439165
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
general exclusion criteria
Descripción

Exclusion Criteria General

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0205246
1. known sensitivity to pimecrolimus, the polymer (plga) or cobalt chromium.
Descripción

Hypersensitivity Pimecrolimus | Hypersensitivity PLGA | Hypersensitivity Cobalt-Chromium

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1099414
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0071599
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0008576
2. planned treatment with any other pci device in the target vessel(s).
Descripción

Planned Treatment Percutaneous Coronary Intervention Device Target vessel

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3641097
UMLS CUI [1,2]
C1532338
UMLS CUI [1,3]
C0025080
UMLS CUI [1,4]
C0449618
3. mi within 72 hours prior to the index procedure
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
4. the patient is in cardiogenic shock.
Descripción

Shock, Cardiogenic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0036980
5. cerebrovascular accident (cva) within the past 6 months.
Descripción

Cerebrovascular accident

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
6. acute or chronic renal dysfunction
Descripción

Renal dysfunction | Renal dysfunction chronic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3279454
UMLS CUI [2,1]
C3279454
UMLS CUI [2,2]
C0205191
7. contraindication to asa or to clopidogrel.
Descripción

Medical contraindication Aspirin | Medical contraindication clopidogrel

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0004057
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0070166
8. thrombocytopenia
Descripción

Thrombocytopenia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0040034
9. active gastrointestinal (gi) bleeding within the past 3 months.
Descripción

Gastrointestinal Hemorrhage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0017181
10. any prior true anaphylactiod reaction to contrast agents
Descripción

Anaphylactoid reaction Contrast Media

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0340865
UMLS CUI [1,2]
C0009924
11. patient is currently taking chronic systemic steroid therapy or systemic immunosuppressant therapy or topical pimecrolimus.
Descripción

systemic steroids chronic | Therapeutic immunosuppression Systemic | Pimecrolimus Topical

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2825233
UMLS CUI [1,2]
C0205191
UMLS CUI [2,1]
C0021079
UMLS CUI [2,2]
C0205373
UMLS CUI [3]
C3213133
12. female of childbearing potential.
Descripción

Childbearing Potential

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3831118
13. life expectancy of less than 24 months due to other medical conditions.
Descripción

Life Expectancy Due to Other medical condition

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C3843040
14. co-morbid condition(s)
Descripción

Comorbidity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009488
15. currently participating in another investigational drug or device study
Descripción

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570

Similar models

Eligibility Coronary Disease NCT00322543

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Inclusion criteria General
Item
general inclusion criteria
boolean
C1512693 (UMLS CUI [1,1])
C0205246 (UMLS CUI [1,2])
Eligibility Percutaneous Coronary Intervention
Item
1. eligible for percutaneous coronary intervention (pci).
boolean
C0680253 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
Stable angina | Angina, Unstable
Item
2. documented stable or unstable angina pectoris
boolean
C0340288 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
Left ventricular ejection fraction
Item
3. left ventricular ejection fraction (lvef) ≥25%
boolean
C0428772 (UMLS CUI [1])
Indication Coronary Artery Bypass Surgery
Item
4. acceptable candidate for coronary artery bypass graft surgery (cabg).
boolean
C3146298 (UMLS CUI [1,1])
C0010055 (UMLS CUI [1,2])
Target Lesion Length | Reference Vessel Diameter | Stenosis Percentage
Item
5. target lesion < 25 mm in length with rvd of 2.5 to 3.5 mm with visually estimated stenosis of >= 50 and < 100 %.
boolean
C2986546 (UMLS CUI [1,1])
C1444754 (UMLS CUI [1,2])
C1706462 (UMLS CUI [2,1])
C0005847 (UMLS CUI [2,2])
C1301886 (UMLS CUI [2,3])
C1261287 (UMLS CUI [3,1])
C0439165 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Exclusion Criteria General
Item
general exclusion criteria
boolean
C0680251 (UMLS CUI [1,1])
C0205246 (UMLS CUI [1,2])
Hypersensitivity Pimecrolimus | Hypersensitivity PLGA | Hypersensitivity Cobalt-Chromium
Item
1. known sensitivity to pimecrolimus, the polymer (plga) or cobalt chromium.
boolean
C0020517 (UMLS CUI [1,1])
C1099414 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0071599 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0008576 (UMLS CUI [3,2])
Planned Treatment Percutaneous Coronary Intervention Device Target vessel
Item
2. planned treatment with any other pci device in the target vessel(s).
boolean
C3641097 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C0025080 (UMLS CUI [1,3])
C0449618 (UMLS CUI [1,4])
Myocardial Infarction
Item
3. mi within 72 hours prior to the index procedure
boolean
C0027051 (UMLS CUI [1])
Shock, Cardiogenic
Item
4. the patient is in cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Cerebrovascular accident
Item
5. cerebrovascular accident (cva) within the past 6 months.
boolean
C0038454 (UMLS CUI [1])
Renal dysfunction | Renal dysfunction chronic
Item
6. acute or chronic renal dysfunction
boolean
C3279454 (UMLS CUI [1])
C3279454 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
Medical contraindication Aspirin | Medical contraindication clopidogrel
Item
7. contraindication to asa or to clopidogrel.
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
Thrombocytopenia
Item
8. thrombocytopenia
boolean
C0040034 (UMLS CUI [1])
Gastrointestinal Hemorrhage
Item
9. active gastrointestinal (gi) bleeding within the past 3 months.
boolean
C0017181 (UMLS CUI [1])
Anaphylactoid reaction Contrast Media
Item
10. any prior true anaphylactiod reaction to contrast agents
boolean
C0340865 (UMLS CUI [1,1])
C0009924 (UMLS CUI [1,2])
systemic steroids chronic | Therapeutic immunosuppression Systemic | Pimecrolimus Topical
Item
11. patient is currently taking chronic systemic steroid therapy or systemic immunosuppressant therapy or topical pimecrolimus.
boolean
C2825233 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0021079 (UMLS CUI [2,1])
C0205373 (UMLS CUI [2,2])
C3213133 (UMLS CUI [3])
Childbearing Potential
Item
12. female of childbearing potential.
boolean
C3831118 (UMLS CUI [1])
Life Expectancy Due to Other medical condition
Item
13. life expectancy of less than 24 months due to other medical conditions.
boolean
C0023671 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
Comorbidity
Item
14. co-morbid condition(s)
boolean
C0009488 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
15. currently participating in another investigational drug or device study
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])

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