Ranolazine Cardioprotection in PCI
Stopped early · Phase 2 · Has a placebo group
Conditions studied: Acute Coronary Syndrome
In brief
The investigators will test if upfront dosing of Ranolazine can reduce myocardial biomarker release (CK-MB, Troponin) post percutaneous coronary intervention (PCI).
Key facts
- Study ID
- NCT01767987
- Run by
- Harvey Hahn
- People needed
- 6
- Starts
- 2012-11-01
- Expected to finish
- 2014-04-01
- Last updated by the study team
- 2017-09-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18 or older
- Patients undergoing Coronary Angiography with possible PCI
- Able and willing to give consent
- Able to read and write English
You may not qualify if…
- Current EKG or Biomarker of Acute Myocardial Infarction (MI) or Acute Coronary Syndromes (ACS)
- History of Allergy to Ranolazine
- Pregnant or Nursing
- Currently taking Ranolazine
Where it is running
- Kettering Medical Center — Kettering, Ohio, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.