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PCI and Renal Denervation in Hypertensive Patients With Acute Coronary Syndromes

Combined Treatment With Percutaneous Coronary Intervention and Renal Denervation in Hypertensive Patients With Acute Coronary Syndromes.

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02272920
Acronym
COMBI-RDN
Enrollment
40
Registered
2014-10-23
Start date
2014-10-31
Completion date
2016-03-31
Last updated
2014-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction, Hypertension

Brief summary

Research hypothesis: Is the treatment with renal denervation (RDN) early post ACS safe and effective and does it leads to improved cardiac function and attenuation of pathologic left ventricular remodelling? In a following study, the hypothesis will be tested in a larger ACS population with major adverse cardiovascular events (MACE) after ACS as the endpoint. Rationale for conducting this study: ACS i.e. ST-elevation myocardial infarction (STEMI) and non- ST-elevation myocardial infarction (non-STEMI) are the most important causes of morbidity and mortality in western societies. Hypertension is a major risk factor for development of ACS and heart failure but it also worsens the prognosis in patients after ACS. Our research highlights the combination therapy of PCI and RDN in an ACS patient population with simultaneous hypertension. Primary objective: The primary objective of this study is to establish safety and efficacy of combined treatment with PCI and renal denervation (RDN) in hypertensive patients with acute coronary syndromes (STEMI and non-STEMI ) having ventricular mass after 4 months as the primary variable. Endpoints: The primary end point is change in left ventricular mass (LVM) at 4 months evaluated by magnetic resonance imaging (MRI). Secondary endpoints:, blood pressure (office and 24-h ABPM), and left ventricular volumes and ejection fraction.

Detailed description

The sympathetic nervous system plays a crucial role in the development and progression of hypertension and its adverse consequences. Despite the availability of numerous effective pharmacologic treatments, adequate blood pressure control is not achieved in a large number of subjects. Patients with essential hypertension generally have increased efferent sympathetic drive to the kidneys and an increased rate of sympathetic-nerve firing, possibly modulated by afferent signalling from renal sensory nerves. Recently developed endovascular catheter technology enables selective denervation of the human kidney. A safety and feasibility trial of this procedure identified substantial reductions of blood pressure without substantial procedure-related complications. The therapeutic value seems to be present not only in hypertension but may also be of interest in many clinical conditions e.g. heart failure, chronic end-stage renal disease and insulin resistance and diabetes. The present study (COMBI-RDN) is a randomised clinical trial in 40 patients to investigate safety and efficacy of the combination of Percutan Coronar Interventiom (PCI) and renal denervation (RDN) where RDN is performed early after acute coronary syndrome (ACS). This study is considered a pilot study to evaluate efficacy and safety in patients with ACS. In a second phase there will be a randomised, multicenter study in approximately 2500 patients to demonstrate whether RDN early post ACS could decrease major adverse cardiovascular events in hypertensive patients with ACS. Research hypothesis Is the treatment with renal denervation (RDN) early post ACS safe and effective and does it leads to improved cardiac function and attenuation of pathologic left ventricular remodelling?

Interventions

PROCEDURERenal denervation

Medtronic Symplicity Flex, Medtronic Symplicity Spyral, or St Jude EnligHTN.

Sponsors

Sahlgrenska University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Provision of informed consent prior to any study specific procedures 2. Female and/or male aged 18-80 years 3. Patients with ACS, i.e. STEMI, non-STEMI, treated with PCI 4. Medical history of treated (ongoing) hypertension, or hypertension discovered at the time of ACS, and office SBP \>140 despite treatment with three antihypertensive drugs. 5. Ejection fraction \>40%.

Exclusion criteria

1. Increased risk of pathological bleedings 2. Office systolic blood pressure \<120 3. Renal artery abnormalities. 4. eGFR \<30 mL/min 5. ICD or pacemaker, or any other metallic implant not compatible with MRI 6. Estimated survival time \<1 year 7. Not oriented to person, place and time 8. Inability to understand given information about the study 9. Fertile female

Design outcomes

Primary

MeasureTime frameDescription
Left ventricular remodellingAt 4 months.Change in left ventricular mass and volumes, as measured by magnetic resonance. Comparing intervention and control group.

Secondary

MeasureTime frameDescription
Office and 24-h ambulatory blood pressureAt 4 months after renal denervation.Change in blood pressure. Comparing intervention and control group.

Countries

Sweden

Contacts

Primary ContactBert Andersson, Prof, MD
bert.andersson@vgregion.se+46313427537
Backup ContactElmir Omerovic, MD PhD
elmir.omerovic@wlab.gu.se+46313427560

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026