RecruitingNot ApplicableNCT06447740

Fractional Flow Reserve-guided Stenting Versus Medical Therapy in Atherosclerosis Renal Artery Stenosis

Fractional Flow Reserve-guided Percutaneous Renal Artery Stenting Plus Optimal Medical Therapy Versus Optimal Medical Therapy Alone In Atherosclerosis Renal-vascular Hypertension Patients: a Multicenter Randomized Trial


Sponsor

Peking University First Hospital

Enrollment

200 participants

Start Date

Jun 3, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Although randomized trials have demonstrated there is no benefit of renal-artery stenting in addition to medical therapy for patients with atherosclerosis renal artery stenosis, many patients indeed gained benefit in daily practices after stenting, such as reduction in blood pressure and recovery in renal functions. One important gap is that there is no universal standard to determine whether to stent in these patients. Fraction Flow Reserve (FFR) has been studied for many year in chronic coronary heart disease and FFR-guided revascularization strategy is known to be better than both angiography-guided revascularization and medication alone. Based on the primary finding of FAIR-pilot study (NCT05732077), FFR-guided renal artery stenting is practical. The overall purpose of the FAIR trial is to compare the clinical outcomes and safety of FFR-guided stenting plus optimal medical treatment (OMT) versus OMT alone in patients with renal-vascular hypertensive patients. With the 'all comers' design, participants met the inclusive/exclusive criteria will be enrolled, and hyperemic FFR induced by dopamine will be measured in all participants. If FFR is ≥0.80, patients will be treated with OMT alone and follow up. If FFR is \<0.80, participants will be randomized to stenting in the renal artery plus OMT or OMT alone on a 1:1 ratio. The blood pressure and anti-hypertensive medications will be compared before and 3 months after the procedure based on ambulatory blood pressure monitoring, all participants will be followed up for 1 year.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study compares two approaches for treating narrowing of the kidney arteries (renal artery stenosis) that is causing difficult-to-control high blood pressure: placing a stent guided by blood flow measurement versus using medications alone. **You may be eligible if...** - You have high blood pressure that is not controlled despite taking 2 or more blood pressure medications - You have been found to have renal artery stenosis (50–90% narrowing) through imaging - Your kidney artery is at least 4mm in diameter **You may NOT be eligible if...** - Your blood pressure is dangerously high (systolic ≥200 mmHg) - You have only one functioning kidney - You have had a prior kidney artery procedure Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDopamine

A bolus dose of 50μg/kg dopamine via renal artery to induce hyperemic status

DIAGNOSTIC_TESTFractional Flow Reserve, Renal

Renal FFR will be measured based on SOP

DEVICERenal artery stenting

Renal artery stenting will be implanted based on the protocol


Locations(1)

Peking University First Hospital

Beijing, Beijing Municipality, China

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NCT06447740


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