Optical coherence tomography to guide stent placement during percutaneous coronary interventio
- Conditions
- Topic: Cardiovascular diseaseSubtopic: Cardiovascular (all Subtopics)Disease: CardiovascularCirculatory System
- Registration Number
- ISRCTN22628285
- Lead Sponsor
- niversity Hospitals Bristol NHS Foundation Trust
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Stopped
- Sex
- All
- Target Recruitment
- 128
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
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
10. Additional significant disease (>50% stenosis) in same vessel proximal or distal to culprit lesion
11. Target vessels / lesions of excessive tortuosity
12. Patients participating in another interventional study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method