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Clinical Trials/NCT01118481
NCT01118481CompletedNot Applicable

ADenosine Vasodilator Independent Stenosis Evaluation Study (ADVISE)

Imperial College London1 site in 1 country157 target enrollmentStarted: January 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
157
Locations
1
Primary Endpoint
Correlation and descriptive characteristics between adenosine free measure of stenosis severity and FFR

Study Overview

Brief Summary

Narrowing of coronary arteries interferes with blood flow and can cause chest pain. Cardiologists sometimes quantify the extent of the narrowing by measuring the fractional flow reserve (the ratio of the pressure in the aorta to the pressure downstream of the narrowing under conditions of maximal flow). We propose a new technique based on principles of wave intensity analysis (WIA) to better assess coronary stenosis and the significance of the narrowing without the need for administration of vasodilator agents such as adenosine. This would simplify assessment and improve our ability to advise patients whether stent treatment will help their symptoms.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

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

Inclusion Criteria

  • Patients with coronary stenosis

Exclusion Criteria

  • Patient's with cardiac pacemakers, valvular heart disease, and chronic renal failure
  • Unable to consent
  • Contraindications to adenosine
  • Contraindications to cardiac MRI

Outcomes

Primary Outcomes

Correlation and descriptive characteristics between adenosine free measure of stenosis severity and FFR

Time Frame: Study end

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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