ID

38496

Beschrijving

Care China-Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00938119

Link

https://clinicaltrials.gov/show/NCT00938119

Trefwoorden

Versies (1)
  1. 22-10-19 22-10-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

22 oktober 2019

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 Cardiovascular Disease NCT00938119

Engels

Eligibility Cardiovascular Disease NCT00938119

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients between the ages of 18 and 80 (inclusive) receiving cypher select™+
Beschrijving

Age | Other Coding | Sirolimus drug-eluting stent Trademark name Specified

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C3846158
UMLS CUI [3,1]
C2199093
UMLS CUI [3,2]
C3242373
UMLS CUI [3,3]
C0205369
sirolimus-eluting coronary stent according to standard clinical practice when financially feasible
Beschrijving

Sirolimus drug-eluting stent Coronary

Datatype

boolean

Alias
UMLS CUI [1,1]
C2199093
UMLS CUI [1,2]
C1522318
the patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate institutional review board/ethics committee of the respective clinical site.
Beschrijving

Protocol Compliance | Protocol Compliance Legal Guardian | Informed Consent | Informed Consent Legal Guardian

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C0023226
UMLS CUI [3]
C0021430
UMLS CUI [4,1]
C0021430
UMLS CUI [4,2]
C0023226
patient has diagnosis of diabetes or is diagnosed with it before or during the index procedure hospitalization based on disease diagnosis criteria
Beschrijving

Diabetes Mellitus | Hospitalization

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0019993
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
any contraindication to any of the following medications: aspirin, heparin, thienopyridines (clopidogrel/ticlopidine), stainless steel, contrast agents, or sirolimus
Beschrijving

Medical contraindication Aspirin | Medical contraindication Heparin | Medical contraindication Thienopyridines | Medical contraindication Clopidogrel | Medical contraindication Ticlopidine | Medical contraindication Stainless Steel | Medical contraindication Contrast Media | Medical contraindication Sirolimus

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0004057
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0019134
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C2936588
UMLS CUI [4,1]
C1301624
UMLS CUI [4,2]
C0070166
UMLS CUI [5,1]
C1301624
UMLS CUI [5,2]
C0040207
UMLS CUI [6,1]
C1301624
UMLS CUI [6,2]
C0038126
UMLS CUI [7,1]
C1301624
UMLS CUI [7,2]
C0009924
UMLS CUI [8,1]
C1301624
UMLS CUI [8,2]
C0072980
an elective surgical procedure is planned that would necessitate interruption of antiplatelet drugs during the first 6 months post enrollment
Beschrijving

Elective Surgical Procedure Planned | Requirement Interruption Antiplatelet Agents

Datatype

boolean

Alias
UMLS CUI [1,1]
C0206058
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C1514873
UMLS CUI [2,2]
C1512900
UMLS CUI [2,3]
C0085826
cardiogenic shock
Beschrijving

Shock, Cardiogenic

Datatype

boolean

Alias
UMLS CUI [1]
C0036980
terminal illness with life expectancy <1 year
Beschrijving

Terminal illness | Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0679247
UMLS CUI [2]
C0023671
st-segment elevation myocardial infarction within 7 days prior to the index procedure
Beschrijving

ST segment elevation myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1]
C1536220
any patient who received coronary stent(s) within 1 year
Beschrijving

Coronary stent Received Recently

Datatype

boolean

Alias
UMLS CUI [1,1]
C0687568
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0332185
Terug naar het begin van de pagina

Similar models

Eligibility Cardiovascular Disease NCT00938119

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age | Other Coding | Sirolimus drug-eluting stent Trademark name Specified
Item
patients between the ages of 18 and 80 (inclusive) receiving cypher select™+
boolean
C0001779 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
C2199093 (UMLS CUI [3,1])
C3242373 (UMLS CUI [3,2])
C0205369 (UMLS CUI [3,3])
Sirolimus drug-eluting stent Coronary
Item
sirolimus-eluting coronary stent according to standard clinical practice when financially feasible
boolean
C2199093 (UMLS CUI [1,1])
C1522318 (UMLS CUI [1,2])
Protocol Compliance | Protocol Compliance Legal Guardian | Informed Consent | Informed Consent Legal Guardian
Item
the patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate institutional review board/ethics committee of the respective clinical site.
boolean
C0525058 (UMLS CUI [1])
C0525058 (UMLS CUI [2,1])
C0023226 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3])
C0021430 (UMLS CUI [4,1])
C0023226 (UMLS CUI [4,2])
Diabetes Mellitus | Hospitalization
Item
patient has diagnosis of diabetes or is diagnosed with it before or during the index procedure hospitalization based on disease diagnosis criteria
boolean
C0011849 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Aspirin | Medical contraindication Heparin | Medical contraindication Thienopyridines | Medical contraindication Clopidogrel | Medical contraindication Ticlopidine | Medical contraindication Stainless Steel | Medical contraindication Contrast Media | Medical contraindication Sirolimus
Item
any contraindication to any of the following medications: aspirin, heparin, thienopyridines (clopidogrel/ticlopidine), stainless steel, contrast agents, or sirolimus
boolean
C1301624 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0019134 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C2936588 (UMLS CUI [3,2])
C1301624 (UMLS CUI [4,1])
C0070166 (UMLS CUI [4,2])
C1301624 (UMLS CUI [5,1])
C0040207 (UMLS CUI [5,2])
C1301624 (UMLS CUI [6,1])
C0038126 (UMLS CUI [6,2])
C1301624 (UMLS CUI [7,1])
C0009924 (UMLS CUI [7,2])
C1301624 (UMLS CUI [8,1])
C0072980 (UMLS CUI [8,2])
Elective Surgical Procedure Planned | Requirement Interruption Antiplatelet Agents
Item
an elective surgical procedure is planned that would necessitate interruption of antiplatelet drugs during the first 6 months post enrollment
boolean
C0206058 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1514873 (UMLS CUI [2,1])
C1512900 (UMLS CUI [2,2])
C0085826 (UMLS CUI [2,3])
Shock, Cardiogenic
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Terminal illness | Life Expectancy
Item
terminal illness with life expectancy <1 year
boolean
C0679247 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
ST segment elevation myocardial infarction
Item
st-segment elevation myocardial infarction within 7 days prior to the index procedure
boolean
C1536220 (UMLS CUI [1])
Coronary stent Received Recently
Item
any patient who received coronary stent(s) within 1 year
boolean
C0687568 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
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