- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01475552
Tailored Antiplatelet Therapy During Percutaneous Coronary Intervention in Patients With Diabetes Mellitus
The Effect of Point-of-care Platelet Function Assay Guided Antiplatelet Therapy on the Periprocedural Increase of Cardiac Enzymes.
The researchers aimed to investigate the effect of point-of-care platelet function assay on the periprocedural cardiac enzyme elevation in patients with diabetes mellitus.
All patients who are supposed to undergo coronary angiography were loaded with clopidogrel (300mg) and aspirin (300mg) at D-1. If patients were determined to implant coronary stent after diagnostic coronary angiography, their platelet function is assayed with Verifynow-ADP (Accumetrics). If patients have >270 unit in the assay, they are randomized to abciximab or control group. After successful stent implantation, cardiac enzymes (CK-MB, Troponin-I) are followed at 8hr, 16hr and 24hr. Clinical outcomes including bleeding complications are assessed at 1 month.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 4
Kontakter och platser
Studieorter
-
-
-
Seongnam, Korea, Republiken av
- Seoul National University Bundang Hospital
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-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Patients who were determined to implant drug-eluting coronary stent
- Diabetes mellitus (type 1 or 2)
Exclusion Criteria:
- Age <18 years or >80years
- Patients with acute myocardial infarction
- Patients with history of cerebral hemorrhage ever or ischemic infarction within 2 years
- Patients with history of major surgery (abdominal, thoracic, intraocular) within 6 months
- Patients who have have allergy to antiplatelet medications (aspirin, clopidogrel, abciximab)
- Patients who are on anticoagulation therapy
- Serum creatinine >2.0mg/dl or ALT/AST > 3 times of upper normal limit (120 U/L)
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: kontrollera
|
Patients,who showed PRU >270 unit and were randomized to control group,were treated with conventional antiplatelet therapy (aspirin+clopidogrel) during PCI and follow up periods. Aspirin : D-1 300mg, D0-30 100mg qd Clopidogrel : D-1 300mg, D0-30 75mg qd
Andra namn:
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Experimentell: abciximab
|
Patients, who showed PRU >270 unit and were randomized to abciximab group,were treated with abciximab in addition to conventional antiplatelet treatment (aspirin+clopidogrel).
Andra namn:
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Peak cardiac enzyme level (CK-MB,troponin-I)
Tidsram: within 24 hrs
|
The investigators will check cardiac enzymes at 8hrs, 16hrs and 24hrs after percutaneous coronary intervention.
We will take the highest value among those measured at three time points as a patient's peak cardiac enzyme level.
The primary outcome of this study is to compare the peak cardiac enzyme level between two groups.
|
within 24 hrs
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
major adverse cardiovascular events (MACE): a composite of cardiac death, myocardial infarction, ischemic stroke
Tidsram: 1 month
|
1 month
|
|
|
Bleeding complications (cerebrovascular, intraocular, bleeding which needs transfusion more than 2 pints)
Tidsram: 1 month
|
1 month
|
|
|
The rate of periprocedural myocardial infarction
Tidsram: 8hr, 16hr, 24hrs
|
The definition of periprocedural myocardial infarction : cardiac enzyme increase more than three times of upper normal limit
|
8hr, 16hr, 24hrs
|
Samarbetspartners och utredare
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Störningar i glukosmetabolism
- Metaboliska sjukdomar
- Sjukdomar i det endokrina systemet
- Diabetes mellitus
- Läkemedels fysiologiska effekter
- Neurotransmittormedel
- Molekylära mekanismer för farmakologisk verkan
- Trombocytaggregationshämmare
- Purinerga P2Y-receptorantagonister
- Purinerga P2-receptorantagonister
- Purinerga antagonister
- Purinerga medel
- Antikoagulantia
- Clopidogrel
- Abciximab
Andra studie-ID-nummer
- DM-Verifynow
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