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Clinical Trials/NCT00967876
NCT00967876CompletedNot Applicable

Coronary Artery Stent Evaluation With 320-slice Computed Tomography - The CArS 320 Study

Charite University, Berlin, Germany1 site in 1 country90 target enrollmentStarted: April 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
90
Locations
1

Study Overview

Brief Summary

The investigators aim at analyzing the diagnostic accuracy of 320-row CT for coronary stents.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
40 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Suspected coronary artery in-stent restenoses based on clinical findings or findings on other noninvasive imaging tests and planned coronary angiography within the next 14 days.
  • Able to understand and willing to sign the Informed CF.

Exclusion Criteria

  • Creatinine of above 2.0 mg/dl
  • Age below 40 years
  • Women of child bearing potential (no hysterectomy, no menopause, or menopause since less than 12 months) must demonstrate a negative pregnancy test performed within 24 hours before CT.
  • Resting heart rate above 70 beats per minute and contraindications to beta blockers (e.g. moderate to severe bronchospastic disease, asthma)
  • Atrial fibrillation, uncontrolled tachycardia, A-V block II or III degree or other non-sinus rhythms
  • Inability to hold the breath for 10 seconds
  • Hypotension < 80 mmHg systolic
  • Unstable angina pectoris, acute myocardial infarction < 48h
  • Continuous therapy with Dipyridamol
  • Severe aortic stenosis

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marc Dewey

PD

Charite University, Berlin, Germany

Study Sites (1)

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