ISRCTN22628285
Terminated
未知
Optical Coherence Tomography to guIde stent placeMent durIng percutaneouS coronary intErvention: a randomised controlled trial
niversity Hospitals Bristol NHS Foundation Trust0 sites128 target enrollmentMarch 11, 2015
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversity Hospitals Bristol NHS Foundation Trust
- Enrollment
- 128
- Status
- Terminated
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A participant may enter study if ALL of the following apply:
- •1\. Adults of either sex aged 30 to 90 years who are undergoing EITHER,
- •1\.1\. Elective PCI for the treatment of CAD OR
- •1\.2\. Urgent PCI for the treatment of ACS
- •2\. Patients who are willing and able to give written informed consent for participation in the study
- •3\. Patients who are anticipated to have at least a 20 mm stent length in at least one lesion
Exclusion Criteria
- •A participant may not enter study if ANY of the following apply:
- •1\. Patients unable to provide written informed consent.
- •2\. Patient undergoing emergency PCI
- •3\. Patients that have had previous PCI within the target vessel.
- •4\. Women who are pregnant or breast feeding
- •5\. Haemodynamic instability
- •6\. Renal impairment (eGFR \=50 ml/min)
- •7\. Multivessel PCI (\>2 vessels) during a single procedure
- •8\. Left main stem disease
- •9\. Estimated angiographic vessel calibre \<2\.5mm or \>4\.5mm
Outcomes
Primary Outcomes
Not specified
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