ID
12467
Beschrijving
The aim of the Mashed Or Just Integral pill of TicagrelOr (MOJITO) study is to evaluate the superiority of Ticagrelor 180 mg LD mashed pill versus Ticagrelor 180 mg LD integral pill both orally administrated in decreasing residual platelet reactivity 1 hour after the administration among 70 patients with STEMI (ST segment elevation myocardial infarction) undergoing PPCI (primary percutaneous coronary intervention) with bivalirudin monotherapy. https://clinicaltrials.gov/ct2/show/NCT01992523
Link
https://clinicaltrials.gov/ct2/show/NCT01992523
Trefwoorden
Versies (2)
- 28-07-15 28-07-15 -
- 21-11-15 21-11-15 -
Geüploaded op
21 november 2015
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Mojito Study Acute Coronary Syndrome NCT01992523
Eligibility Criteria
- StudyEvent: ODM
Beschrijving
Exclusion Criteria
Beschrijving
Age < 18 years or Age > 75 years
Datatype
boolean
Alias
- UMLS CUI-1
- C0001779
Beschrijving
Active bleeding
Datatype
boolean
Alias
- UMLS CUI-1
- C0019080
Beschrijving
bleeding diathesis
Datatype
boolean
Alias
- UMLS CUI-1
- C3251812
Beschrijving
coagulopathy
Datatype
boolean
Alias
- UMLS CUI-1
- C0005779
Beschrijving
Increased risk of bradycardiac events
Datatype
boolean
Alias
- UMLS CUI-1
- C0428977
Beschrijving
History of gastrointestinal bleeding <2 months
Datatype
boolean
Alias
- UMLS CUI-1
- C0017181
Beschrijving
History of genitourinary bleeding <2 months
Datatype
boolean
Alias
- UMLS CUI-1
- C0919591
Beschrijving
Major surgery in the last 6 weeks
Datatype
boolean
Alias
- UMLS CUI-1
- C0679637
Beschrijving
History of intracranial bleeding or structural abnormalities
Datatype
boolean
Alias
- UMLS CUI-1
- C0151699
Beschrijving
Suspected aortic dissection
Datatype
boolean
Alias
- UMLS CUI-1
- C0340643
Beschrijving
Administration in the week before the index event of clopidogrel
Datatype
boolean
Alias
- UMLS CUI-1
- C0070166
Beschrijving
Administration in the week before the index event of ticlopidine
Datatype
boolean
Alias
- UMLS CUI-1
- C0040207
Beschrijving
Administration in the week before the index event of prasugrel
Datatype
boolean
Alias
- UMLS CUI-1
- C1620287
Beschrijving
Administration in the week before the index event of ticagrelor
Datatype
boolean
Alias
- UMLS CUI-1
- C1999375
Beschrijving
Administration in the week before the index event of thrombolytics
Datatype
boolean
Alias
- UMLS CUI-1
- C0040044
Beschrijving
Administration in the week before the index event of bivalirudin
Datatype
boolean
Alias
- UMLS CUI-1
- C0168273
Beschrijving
Administration in the week before the index event of low-molecular weight heparin
Datatype
boolean
Alias
- UMLS CUI-1
- C3536766
Beschrijving
Administration in the week before the index event of fondaparinux
Datatype
boolean
Alias
- UMLS CUI-1
- C1098510
Beschrijving
Concomitant oral or IV therapy with strong CYP3A inhibitors
Datatype
boolean
Alias
- UMLS CUI-1
- C3830624
Beschrijving
Concomitant oral or IV therapy with strong CYP3A inducers
Datatype
boolean
Alias
- UMLS CUI-1
- C3830625
Beschrijving
Known relevant hematological deviations: Hb <10 g/dl
Datatype
boolean
Alias
- UMLS CUI-1
- C0518015
Beschrijving
Known relevant hematological deviations: Thrombi. <100x10^9/l
Datatype
boolean
Alias
- UMLS CUI-1
- C0032181
Beschrijving
Use of coumadin derivatives within the last 7 days
Datatype
boolean
Alias
- UMLS CUI-1
- C0043031
Beschrijving
Known severe liver disease
Datatype
boolean
Alias
- UMLS CUI-1
- C0085605
Beschrijving
severe renal failure
Datatype
boolean
Alias
- UMLS CUI-1
- C0035078
Beschrijving
Known allergy to the study medications
Datatype
boolean
Alias
- UMLS CUI-1
- C0013182
Beschrijving
Pregnancy
Datatype
boolean
Alias
- UMLS CUI-1
- C0549206
Similar models
Eligibility Criteria
- StudyEvent: ODM