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Clinical Trials/NCT01701596
NCT01701596
Completed
Phase 1

Safety and Efficacy of Immediate Rotational Atherectomy in Nondilatable Calcified Lesion Complicated by Coronary Dissection (RAISE)

Xijing Hospital1 site in 1 country198 target enrollmentAugust 2004

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Coronary Artery Disease
Sponsor
Xijing Hospital
Enrollment
198
Locations
1
Primary Endpoint
All cause death
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study is aimed at examining the safety and efficacy of rotational atherectomy (RA) in nondilatable calcified lesion complicated by coronary dissection during percutaneous coronary intervention (PCI) procedure.

Detailed Description

Coronary artery dissection is a contraindication for the use of rotational atherectomy, since rotational atherectomy may propagate coronary dissection. In the presence of coronary dissection, conservative management is suggested for approximately 4 weeks to permit the dissection to heal prior to treatment with rotational atherectomy. However, a lot of patients have frequent angina attacks and some patients develop serious complications including abrupt vessel closure during this period. Thus, immediate strategies cope with coronary dissection induced by balloon dilation is needed for the early recovery of those patients. The present study was performed to compare the safety and efficacy of immediate RA and delayed RA in the treatment with nondilatable calcified lesion complicated by coronary dissection.

Registry
clinicaltrials.gov
Start Date
August 2004
End Date
June 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Xijing Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age between 30 and 85 years old
  • nondilatable calcified lesion complicated by coronary dissection during percutaneous coronary intervention (PCI) procedure
  • Coronary artery dissection type A, B and type C according to the National Heart, Lung and Blood Institute (NHLBI) coronary dissection criteria

Exclusion Criteria

  • acute myocardial infarction
  • unprotected left main stenosis
  • chronic total occlusion
  • saphenous vein graft lesion
  • cardiomyopathy
  • severe valvular heart disease
  • NYHA functional class IV heart failure at baseline
  • chronic renal failure on hemodialysis
  • severe lung and liver disease or cancer

Outcomes

Primary Outcomes

All cause death

Time Frame: 4 years

cardiac death and non-cardiac death

Secondary Outcomes

  • Left ventricular ejection fraction (LVEF)(4 years)
  • Stent thrombosis(4 years)
  • New York Heart Association (NYHA) class IV heart failure(4 years)
  • Non-fatal myocardial infarction(4 years)
  • Cardiac tamponade(4 years)
  • Stroke(4 years)
  • 6-min walk distance (6MWD)(4 years)
  • angina class(4 years)
  • Target lesion revascularization(4 years)

Study Sites (1)

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