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Clinical Trials/ISRCTN22628285
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.

Registry
who.int
Start Date
March 11, 2015
End Date
May 1, 2018
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity Hospitals Bristol NHS Foundation Trust

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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