CClinicalTrials.gg
Status unknownNCT03279484NAVIGATORUpdated Sep 17, 2019

Safety and Electrical Performances Evaluation of Navigo Leads Equipped With IS4 Connector

An interventional study of NAVIGO 4LV lead implant in Arrythmia, Implatable Cardioverter Defibrillation, Lead, sponsored by MicroPort CRM. Status unknown at 38 sites in 6 countries. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2019-09-17.

Sponsored by MicroPort CRM · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2019), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
317
Allocation
Not applicable
Ages
18 Years to 100 Years
Sex
All
01

Study summary

The primary objective of this study is to assess the safety and electrical performance of Left ventricular (LV) NAVIGO 4LV leads, pre-shaped (S-shaped\&U-shaped: NAVIGO 4LV 2D, NAVIGO 4LV ARC) and Straight (NAVIGO 4LV PILOT), with IS4 connector

Read the detailed description

The devices under investigation, NAVIGO 4LV models Pilot, 2D , and ARC are the new quadripolar coronary venous leads with polyurethane lead body, intended to be used with defibrillators with ventricular resynchronization therapy.

The new lead design with the presence of 4 electrodes that allows several combinations in programming pacing vectors, is intended to benefit both the patients by improving response to therapy, overcoming high pacing threshold and avoiding phrenic nerve stimulation, and the investigators by reducing the number of re-interventions needed.

This clinical investigation is a pre-market release study intended to analyze safety and electrical performance of NAVIGO 4LV leads pre-shaped (S-shaped \& U-shaped) and Straight leads models. The primary endpoint data will be used to support the achievement of the CE mark of NAVIGO 4LV leads.

The primary endpoints will be evaluated at 1 month post-implantation; secondary endpoints will be evaluated up to 2 years post-implantation. The duration of patient inclusion will be approximately 10 months for pre-shaped NAVIGO family (S-shaped \&U-shaped) and approximately 21 months for straight ones.

The post implant follows-up visits will take place at Hospital discharge, weeks 10, 6 months and every 6 months until 2 years.

02

Conditions studied

  • Arrythmia, Implatable Cardioverter Defibrillation, Lead

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Keywords

  • safety , electrical performance
03

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Any patient presenting a CRT-D indication as detailed in the ESC guidelines
  • Primary implant of a PLATINIUM 4LV CRTD or upgrade from an existing ICD connected to a RV lead with a DF4 connector (DF4LLHH) to a PLATINIUM 4LV CRT-D
  • Signed and dated informed consent

Exclusion criteria

Exclusion Criteria:

  • Patients for whom a maximum single dose of 300 µg dexamethasone sodium phosphate (DSP) eluted from the NAVIGO 4LV lead maybe contraindicated
  • Venous anomalies precluding transvenous implant (contraindication of a Pacemaker or ICD implant)
  • Active myocarditis, pocket and/or lead infection
  • Stroke/myocardiaI infarction one month prior to implant
  • Already included in another clinical study that could confound the results of this study.
  • Inability to meet Follow-up visits at the implanting centre as defined in the investigational plan.
  • Patient less than 18 years old or under guardianship
  • Known pregnancy, women in lactation period or in childbearing age without an adequate contraceptive method (failure rate \< 1%)
  • Drug addiction or abuse
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
317 participants (estimated)

Study arms

  • Experimental
    NAVIGO 4LV implant

    All patients will be attempted to implant or implanted with NAVIGO 4LV lead

    Device: NAVIGO 4LV lead implant

Interventions

  • DeviceNAVIGO 4LV lead implant

    All patients will be attempted to implant or implanted with NAVIGO 4LV lead

05

What researchers measure

Primary outcomes

  1. LV lead Safety at 10 weeks

    Freedom from LV lead-related complications, defined as any investigational device deficiency or any serious adverse device event (SADE) that resulted in patient death or required a re-intervention (not including re-programming) that occurred within 30 days after successful implant of the CRT-D system

    Time frame: 10 weeks after implant

  2. LV lead Performance at 10 weeks

    Successful performance defined as LV pacing threshold at 10 weeks \< 2.5 V/0.5 ms observed on at least one pacing vector and absence of phrenic nerve stimulation at programmed pacing amplitude

    Time frame: 10 weeks after implant

Secondary outcomes

  1. Electrical performance

    LV pacing threshold amplitude (V) and LV pacing impedance (Ohm)

    Time frame: through study completion, an average of 6 month

  2. Rate of patients free from LV lead-related complications

    Freedom from LV lead-related complications defined as any investigational device deficiency or any serious adverse device event (SADE) that resulted in patient death or required a re-intervention (not including re-programming)

    Time frame: through study completion, an average of 6 month

  3. LV lead-related SAEs

    Serious Adverse Event LV related

    Time frame: through study completion, an average of 6 month

  4. Lead handing assessment of NAVIGO 4LV leads through a questionnaire

    A questionnaire on lead handling will track opinion from the investigator, comparing his assessment with this lead to device he is accustomed to implant

    Time frame: Implant

  5. NAVIGO 4LV lead implant success rate on enrolled population

    To report the NAVIGO 4LV lead implant success rate

    Time frame: Enrollment

  6. Number of patients with at least 2 pacing vectors with pacing threshold < 2.5 V at 0.5 ms and no phrenic nerve stimulation

    To report the number of patients with at least 2 pacing vectors with pacing threshold \< 2.5 V at 0.5 ms and no phrenic nerve stimulation

    Time frame: 10 weeks

  7. Number of patients with MP pacing activated

    To report the number of patients with MP pacing activated

    Time frame: through study completion, an average of 6 month

  8. Rationale to activate MP

    To report the reason why physician decide to activate MP to the patient

    Time frame: through study completion, an average of 6 month

  9. Number of patients with of at least one MP configuration with no phrenic nerve stimulation at programmed pacing amplitude

    To report the number of patients with at least one MP configuration with no phrenic nerve stimulation at programmed pacing amplitude

    Time frame: through study completion, an average of 6 month

  10. Number of patients at each final programmed pacing vector and changes

    To report number of patients at each final programmed pacing vector and changes

    Time frame: through study completion, an average of 6 month

06

Study locations

38 sites
  • CHRU Brest
    Brest, 29609, France
  • CHRU Hopital Trousseau
    Chambray-lès-Tours, 37170, France
  • CH Robert Boulin
    Libourne, 33505, France
  • CHU Hôpital Nord - Marseille
    Marseille, 13020, France
  • Institut Hospitalier Jacques Cartier
    Massy, 91349, France
  • CH Annecy Genevois
    Metz-Tessy, 74374, France
  • Groupe Hospitalier Paris St Joseph
    Paris, 75014, France
  • Institut Mutualiste Montsouris
    Paris, 75014, France
  • CHU Bordeaux
    Pessac, 33600, France
  • CHU Hopital Charles Nicolle
    Rouen, 76031, France
  • CHU Rangueil
    Toulouse, 31059, France
  • Centre Hospitalier de Valence
    Valence, 26953, France
  • CHRU Brabois
    Vandoeuvre les Nancy, 54500, France
  • Herz- und Gefässzentrum Bad Bevensen
    Bad Bevensen, 29594, Germany
  • Herz- und Diabeteszentrum
    Bad Oeynhausen, 32545, Germany
  • Deutsches Herzzentrum Berlin
    Berlin, 13353, Germany
  • Evangelisches Krankenhaus
    Bielefeld, 33617, Germany
  • Klinikum Coburg
    Coburg, 96450, Germany
  • Kardiologie Darmstadt
    Darmstadt, 64287, Germany
  • Universitäts-Herzzentrum Freiburg
    Freiburg, 79106, Germany
  • Albertinen-Krankenhau
    Hamburg, 22457, Germany
  • Universitätsklinikum Schleswig-Holstein, Campus Kiel
    Kiel, 24105, Germany
  • Universitatsklinikum
    Wurzburg, 97080, Germany
  • Az. Osp-Univ. Ospedali Riuniti Umberto I-Lancisi-Salesi
    Ancona, 60126, Italy
  • Ospedale Universitario Di Pisa
    Pisa, 56126, Italy
  • Az. Osp. Univ. S. Maria della Misericordia
    Udine, 33100, Italy
  • ISALA Klinieken
    Zwolle, 10500, Netherlands
  • Centro Hospitalar Lisboa Ocidental -Hospital de Santa Cruz (CHLO)
    Carnaxide, 2799, Portugal
  • Centro Hospitalar Universitário de Coimbra -Hospitais da Universidade de Coimbra
    Coimbra, 3000-075, Portugal
  • Centro Hospitalar e Universitário de Coimbra - Hospital Geral
    Coimbra, 3041-801, Portugal
  • Centro H. Lisboa Norte - Hospital de Santa Maria
    Lisboa, 1649-035, Portugal
  • CHCL - Hospital Santa Marta
    Lisbon, 1169-024, Portugal
  • Centro Hospitalar do Porto CHP Hospital de Santo Antonio
    Porto, 4099-001, Portugal
  • Hospital General Universitario de Alicante
    Alicante, 03010, Spain
  • Hospital Universitario Gregorio Marañón
    Madrid, 28007, Spain
  • H. Universitario Central de Asturias
    Oviedo, 33011, Spain
  • Hospital Universitario La Fe
    Valencia, 46009, Spain
  • Complejo Hospitalario Universitario de Vigo - Hospital Alvaro Cunqueiro
    Vigo, 36312, Spain
07

Registry details

Key details

Study ID
NCT03279484
Lead sponsor
MicroPort CRM
Responsible party
Sponsor
First posted
Sep 12, 2017
Start date
Nov 24, 2017
Primary completion
Dec 2019 (estimated)
Completion
Mar 2022 (estimated)
Last update
Sep 17, 2019

Study contacts

Juan Gabriel Martinez Martinez
principal investigator · Hospital General Universitario Alicante Spain

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
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