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Saline-induced Distal to Aortic Coronary Pressure Ratio vs. Resting and Hyperemic Indices of Coronary Artery Stenosis Severity (SALINE)

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University Hospitals (UH)

Status

Completed

Conditions

Coronary Stenosis

Treatments

Procedure: Saline Pd/Pa

Study type

Interventional

Funder types

Other

Identifiers

NCT04284345
2019-00910

Details and patient eligibility

About

The presence of inducible myocardial ischemia is considered as the prerequisite for the clinical benefit of coronary revascularization. In this regard, the introduction of invasive pressure-derived physiological indices to guide myocardial revascularization represented a major breakthrough for the treatment of patients with coronary artery disease (CAD), by moving the focus of coronary revascularization from anatomy to physiology . The main premise of coronary physiology is to permit determination of the functional significance of individual stenoses on a per-vessel basis, measurable at the time of clinical decision-making process, thus providing an objective marker to identify ischemic lesions, and therefore patients, most likely to benefit from coronary revascularization .

Fractional flow reserve (FFR) is the most widely used pressure-derived invasive physiological index for coronary lesion assessment in contemporary clinical practice. FFR is calculated as the ratio of the mean distal coronary pressure (Pd) to the mean proximal coronary pressure (Pa) across a stenosis during maximal hyperaemia, a condition that is commonly achieved by the intracoronary or intravenous administration of a potent vasodilator agent, such as adenosine. Based on the results of landmark clinical trials, most recent guidelines recommend the use of FFR to identify hemodynamically significant coronary lesions in patients with stable CAD. Despite this, the worldwide adoption of FFR into current clinical practice remains limited , accounting for only 9.8% of coronary procedures in Switzerland . Potential reasons for the low adoption rate of coronary physiology include technical challenges and time consumption related to FFR measurements, inadequate or lack of reimbursement, physician preferences, patient-related discomfort, contraindications and costs associated with adenosine, or in certain countries, no availability of adenosine.

The low use of FFR in clinical practice provided a rationale for the development of new invasive physiology indices. By negating the need for administration of pharmacologic agents such as adenosine, saving time, and reducing costs and side effects, hyperaemia-free pressure-derived physiological indices were developed to increase adoption of physiology-guided coronary revascularization into routine clinical practice.

Enrollment

90 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject is ≥18 years of age.
  • Subject must be willing to sign a Patient Informed Consent (PIC).
  • Coronary artery disease with over 50% angiographic diameter stenosis on visual assessment, undergoing clinically indicated invasive physiological assessment by means of FFR.
  • Assessment of non culprit arteries with over 50% angiographic diameter stenosis on visual assessment, in patients presenting with NSTEMI.

Exclusion criteria

  • Pregnant and/or breastfeeding females.
  • Known allergies to: heparin, contrast medium, adenosine.
  • Contra-indication to adenosine.
  • Severe renal failure (eGFR ≤ 30 ml/min/m2).
  • Ostial stenosis in both the left and right coronary arteries.
  • Presence of a chronic total occlusion.
  • History of coronary artery bypass graft.
  • Acute coronary syndrome.
  • Acute myocardial infarction within the preceding two weeks.
  • Severe valvular heart disease.
  • Left main disease.
  • Documented left ventricular ejection fraction (LVEF) ≤30% as documented within maximum 6 months prior to the procedure.
  • Decompensated congestive heart failure.
  • Extreme hypotension (systolic blood pressure <100 mmHg)
  • Extreme bradycardia (<40 bpm).

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

90 participants in 1 patient group

Saline Pd/Pa
Experimental group
Description:
Eligible subjects will undergo invasive coronary physiology measurements including whole cycle resting Pd/Pa, iFR, RFR, cFFR, Saline Pd/Pa and FFR
Treatment:
Procedure: Saline Pd/Pa

Trial contacts and locations

1

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Central trial contact

Sophie Degrauwe, MD; Juan F Iglesias, MD

Data sourced from clinicaltrials.gov

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