ID

28752

Beschrijving

Platelet Reactivity After Cessation of Clopid in the Setting of Coronary Stent Implantation I: PRACTICE I; ODM derived from: https://clinicaltrials.gov/show/NCT00684359

Link

https://clinicaltrials.gov/show/NCT00684359

Trefwoorden

Versies (1)
  1. 01-02-18 01-02-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

1 februari 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Coronary Disease NCT00684359

Engels

Eligibility Coronary Disease NCT00684359

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients, male or female, > 18 years of age,
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients who are scheduled for an elective pci with a drug eluting stent
Beschrijving

Percutaneous Coronary Intervention elective Scheduled | PCI Drug-Eluting Stent

Datatype

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0439608
UMLS CUI [1,3]
C0205539
UMLS CUI [2,1]
C1532338
UMLS CUI [2,2]
C1322815
patients willing to return for all required follow up visits.
Beschrijving

Follow-up visit Willing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0589121
UMLS CUI [1,2]
C0600109
patients live/work within a 60 mile radius of the washington hospital center.
Beschrijving

Residence Nearby Hospital | Working Nearby Hospital

Datatype

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C1706276
UMLS CUI [1,3]
C0019994
UMLS CUI [2,1]
C0043227
UMLS CUI [2,2]
C1706276
UMLS CUI [2,3]
C0019994
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient has experienced an acute myocardial infarction within the preceding 48 hours of the subsequent angioplasty.
Beschrijving

Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
unprotected left main coronary disease with >50% stenosis;
Beschrijving

Left main coronary artery disease Without Protection | Stenosis Percentage

Datatype

boolean

Alias
UMLS CUI [1,1]
C1299433
UMLS CUI [1,2]
C0332288
UMLS CUI [1,3]
C1545588
UMLS CUI [2,1]
C1261287
UMLS CUI [2,2]
C0439165
patients with renal failure requiring dialysis;
Beschrijving

Kidney Failure Requirement Dialysis

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035078
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0011946
patients with a documented ejection fraction < 30 percent at the time of subsequent pci;
Beschrijving

Cardiac ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0232174
patient with a life expectancy less than 12 months or malignancy.
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
known allergies to aspirin or clopidogrel bisulfate (plavixr) and that cannot be medically managed;
Beschrijving

Aspirin allergy | Hypersensitivity Clopidogrel bisulfate | Hypersensitivity Plavix | Allergy prophylaxis Unsuccessful

Datatype

boolean

Alias
UMLS CUI [1]
C0004058
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0772326
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0633084
UMLS CUI [4,1]
C1737226
UMLS CUI [4,2]
C1272705
planned surgery or other indication for requiring the cessation of clopidogrel within 12 months of pci;
Beschrijving

Operative Surgical Procedures Planned | Clopidogrel To be stopped | Indication Clopidogrel To be stopped

Datatype

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0070166
UMLS CUI [2,2]
C1272691
UMLS CUI [3,1]
C3146298
UMLS CUI [3,2]
C0070166
UMLS CUI [3,3]
C1272691
any significant medical condition which in the investigator's opinion may interfere with the patient's optimal participation in the study.
Beschrijving

Medical condition Interferes with Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2348568
patients with known history of bleeding diathesis;
Beschrijving

Bleeding tendency

Datatype

boolean

Alias
UMLS CUI [1]
C1458140
prothrombin time >1.5 times control; coumadin therapy
Beschrijving

Prothrombin time increased | Coumadin

Datatype

boolean

Alias
UMLS CUI [1]
C0151872
UMLS CUI [2]
C0699129
platelet count <100 000/mm3;
Beschrijving

Platelet Count measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0032181
hematocrit <25%;
Beschrijving

Hematocrit procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0018935
creatinine >4.0 mg/dl;
Beschrijving

Creatinine measurement, serum

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
thienopyridine use within 5 days of enrollment
Beschrijving

thienopyridine

Datatype

boolean

Alias
UMLS CUI [1]
C1120149
glycoprotein (gp) iib/iiia use within 8 hours of enrollment or any indication were the operator will require gp iib/iiia inhibitor use during the hospitalization.
Beschrijving

Glycoprotein GPIIb-IIIa | Patient need for Platelet Glycoprotein IIb/IIIA Inhibitors

Datatype

boolean

Alias
UMLS CUI [1]
C0016011
UMLS CUI [2,1]
C0686904
UMLS CUI [2,2]
C1373125
Terug naar het begin van de pagina

Similar models

Eligibility Coronary Disease NCT00684359

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
patients, male or female, > 18 years of age,
boolean
C0001779 (UMLS CUI [1])
Percutaneous Coronary Intervention elective Scheduled | PCI Drug-Eluting Stent
Item
patients who are scheduled for an elective pci with a drug eluting stent
boolean
C1532338 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C1532338 (UMLS CUI [2,1])
C1322815 (UMLS CUI [2,2])
Follow-up visit Willing
Item
patients willing to return for all required follow up visits.
boolean
C0589121 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Residence Nearby Hospital | Working Nearby Hospital
Item
patients live/work within a 60 mile radius of the washington hospital center.
boolean
C0237096 (UMLS CUI [1,1])
C1706276 (UMLS CUI [1,2])
C0019994 (UMLS CUI [1,3])
C0043227 (UMLS CUI [2,1])
C1706276 (UMLS CUI [2,2])
C0019994 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Myocardial Infarction
Item
patient has experienced an acute myocardial infarction within the preceding 48 hours of the subsequent angioplasty.
boolean
C0027051 (UMLS CUI [1])
Left main coronary artery disease Without Protection | Stenosis Percentage
Item
unprotected left main coronary disease with >50% stenosis;
boolean
C1299433 (UMLS CUI [1,1])
C0332288 (UMLS CUI [1,2])
C1545588 (UMLS CUI [1,3])
C1261287 (UMLS CUI [2,1])
C0439165 (UMLS CUI [2,2])
Kidney Failure Requirement Dialysis
Item
patients with renal failure requiring dialysis;
boolean
C0035078 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0011946 (UMLS CUI [1,3])
Cardiac ejection fraction
Item
patients with a documented ejection fraction < 30 percent at the time of subsequent pci;
boolean
C0232174 (UMLS CUI [1])
Life Expectancy
Item
patient with a life expectancy less than 12 months or malignancy.
boolean
C0023671 (UMLS CUI [1])
Aspirin allergy | Hypersensitivity Clopidogrel bisulfate | Hypersensitivity Plavix | Allergy prophylaxis Unsuccessful
Item
known allergies to aspirin or clopidogrel bisulfate (plavixr) and that cannot be medically managed;
boolean
C0004058 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0772326 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0633084 (UMLS CUI [3,2])
C1737226 (UMLS CUI [4,1])
C1272705 (UMLS CUI [4,2])
Operative Surgical Procedures Planned | Clopidogrel To be stopped | Indication Clopidogrel To be stopped
Item
planned surgery or other indication for requiring the cessation of clopidogrel within 12 months of pci;
boolean
C0543467 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0070166 (UMLS CUI [2,1])
C1272691 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3,1])
C0070166 (UMLS CUI [3,2])
C1272691 (UMLS CUI [3,3])
Medical condition Interferes with Study Subject Participation Status
Item
any significant medical condition which in the investigator's opinion may interfere with the patient's optimal participation in the study.
boolean
C3843040 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
Bleeding tendency
Item
patients with known history of bleeding diathesis;
boolean
C1458140 (UMLS CUI [1])
Prothrombin time increased | Coumadin
Item
prothrombin time >1.5 times control; coumadin therapy
boolean
C0151872 (UMLS CUI [1])
C0699129 (UMLS CUI [2])
Platelet Count measurement
Item
platelet count <100 000/mm3;
boolean
C0032181 (UMLS CUI [1])
Hematocrit procedure
Item
hematocrit <25%;
boolean
C0018935 (UMLS CUI [1])
Creatinine measurement, serum
Item
creatinine >4.0 mg/dl;
boolean
C0201976 (UMLS CUI [1])
thienopyridine
Item
thienopyridine use within 5 days of enrollment
boolean
C1120149 (UMLS CUI [1])
Glycoprotein GPIIb-IIIa | Patient need for Platelet Glycoprotein IIb/IIIA Inhibitors
Item
glycoprotein (gp) iib/iiia use within 8 hours of enrollment or any indication were the operator will require gp iib/iiia inhibitor use during the hospitalization.
boolean
C0016011 (UMLS CUI [1])
C0686904 (UMLS CUI [2,1])
C1373125 (UMLS CUI [2,2])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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