Optimization of Coronary Sinus Lead Placement Targeted to the Longest Right-to-Left Delay

NCT ID: NCT03204864

Last Updated: 2018-09-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 211 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-03-01
• Study Completion Date: 2018-03-31

Brief Summary

This study is a prospective, multi-center, physician-initiated study, with intra-center control arm of patients with advanced heart failure undergoing cardiac resynchronization therapy (CRT) with or without defibrillator therapy.

The purpose of this study is to verify whether optimizing the left ventricular lead position at implantation with the pacing cathode corresponding to the longest RV-to-LV electrical delay may result in a better patient outcome. The RV-to-LV electrical delay will be evaluated with RLD value (ms). RLD is the distance between the Right Ventricular pacing marker (VP) and the maximum peak (or the first maximum peak in case of two equally tall peaks) of the LV bipolar deflection.

Detailed Description

This study is a prospective, multi-center, physician-initiated study, with intra-center control arm of patients with advanced heart failure undergoing cardiac resynchronization therapy (CRT) with or without defibrillator therapy.

Approximately 300 patients will be included in the study and followed-up for 6 months. Patients recruitment will consist of two sequential phases:

Phase 1 - Conventional CS lead placement (Conventional subgroup). The first 100 patients will be implanted with a CRT device with or without defibrillator (P/D) as per standard clinical practice, without CS lead pacing specific optimization. In these patients RLD is measured blind to implanting physician who will place CS lead according to his/her clinical practice. Since these patients follow strictly standard clinical practice, their implantation data can be collected prospectively or even retrospectively when available.

Phase 2 - Targeted CS lead placement (RLD subgroup). In the second 200 patients CS placement will be guided by RLD measurement. Physician will place the CS lead in the site of longest RLD with a stable and acceptable pacing threshold.

Conditions

HF Patient

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Conventional CS lead placement

Patients will be implanted with a CRT device with or without defibrillator (P/D) as per standard clinical practice, without CS lead pacing specific optimization.

Group Type: ACTIVE_COMPARATOR

Conventional CS lead placement

Intervention Type: DEVICE

Clinical Practice

RLD Group

Patients CS placement will be guided by RLD measurement. Physician will place the CS lead in the site of longest RLD with a stable and acceptable pacing threshold.

Group Type: EXPERIMENTAL

RLD Group

Intervention Type: DEVICE

patients CS placement will be guided by RLD measurement. Physician will place the CS lead in the site of longest RLD with a stable and acceptable pacing threshold.

Interventions

RLD Group

patients CS placement will be guided by RLD measurement. Physician will place the CS lead in the site of longest RLD with a stable and acceptable pacing threshold.

Intervention Type: DEVICE

Conventional CS lead placement

Clinical Practice

Intervention Type: DEVICE

Other Intervention Names

CRT; CRT

Eligibility Criteria

Inclusion Criteria

• Be in NYHA II or III functional class with approved class I or II standard indications by ESC/EHRA Guidelines
• Either patients in sinus rhythm or in atrial fibrillation. In this latter case patients must perform AV node ablation if complete biventricular stimulation cannot be achieved in >95% of beats
• Patients willing and able to comply with study requirements(patients must indicate their understanding of the study and willingness to participate by signing an appropriate informed consent form)
• Successful LV lead implant

Exclusion Criteria

• Myocardial Infarction, unstable angina within 40 days prior the enrollment
• Recent cardiac revascularization (PTCA, Stent or CABG) in the 4 weeks prior to enrollment or planned for the 3 months following
• Cerebrovascular Accident (CVA) or Transient Ischemic Attack (TIA) in the 3 months prior the enrollment
• Primary valvular disease
• Unable to comply with the follow up schedule
• Less than 18 years of age
• Pregnant or are planning to become pregnant during the duration of the investigation
• Classification of Status 1 for cardiac transplantation or consideration for transplantation over the next 12 months
• Undergone a cardiac transplantation
• Life expectancy < 12 months

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Michele Brignole

OTHER

Sponsor Role: lead

Responsible Party

Michele Brignole

MD

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Michele Brignole, MD

Role: PRINCIPAL_INVESTIGATOR

Ospedale del Tigullio

Locations

Ospedale Villa Scassi

Genova, , Italy

Ospedale di Imperia

Imperia, , Italy

Ospedale del Tigullio-Polo di Lavagna

Lavagna, , Italy

Ospedale di Massa

Massa, , Italy

Countries

Italy

References

Oddone D, Solari D, Arena G, Mureddu R, Nangah R, Giorgi D, Senatore G, Bottoni N, Giaccardi M, Laffi M, Giammaria M, Sitta N, Marras E, Cipolla E, Di Lorenzo F, Carpi R, Brignole M. Optimization of coronary sinus lead placement targeted to right-to-left delay in patients undergoing cardiac resynchronization therapy. Europace. 2019 Mar 1;21(3):502-510. doi: 10.1093/europace/euy275.

Reference Type: DERIVED

PMID: 30508076 (View on PubMed)

Other Identifiers

Ver 5.0

Identifier Type: -

Identifier Source: org_study_id