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Clinical Trials/NCT00176358
NCT00176358
Unknown
Phase 2

Percutaneous Coronary Angioplasty Compared With Exercise Training in Symptomatic Coronary Artery Disease

University of Leipzig1 site in 1 country400 target enrollmentSeptember 15, 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
CAD
Sponsor
University of Leipzig
Enrollment
400
Locations
1
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to compare coronary angioplasty with stent implantation with an exercise rehabilitation program in patients with stable coronary artery disease (CAD).

Registry
clinicaltrials.gov
Start Date
September 15, 2005
End Date
TBD
Last Updated
18 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Leipzig

Eligibility Criteria

Inclusion Criteria

  • Angiographically documented CAD, with at least one coronary artery stenosis of more than 50% in a native segment never subjected to intervention, which is recommended for treatment with percutaneous transluminal coronary angioplasty (PTCA).
  • Stable coronary artery disease
  • Eligible patients could be asymptomatic or have class I to III angina (Canadian Cardiovascular Society \[CCS\]) with documented myocardial ischemia
  • Angina pectoris threshold \> 50 Watt (cycle ergometry)
  • Permanent residence should be within 25 km of training facility.

Exclusion Criteria

  • \< 18 or \> 70 years of age
  • Patient currently participating in an exercise training program
  • Unstable angina pectoris or myocardial infarction during the last 2 weeks
  • Symptoms of CCS class IV
  • Exercise limitations due to clinical conditions not related to CAD
  • Left ventricular ejection fraction (LVEF) of \< 40%
  • Ventricular arrhythmia (Lown Ivb)
  • Hemodynamically significant valvular heart disease
  • Previous cardiac surgery
  • PTCA performed during the last 12 months

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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