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Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT) Candidates (TRIV)

Primary Purpose

Heart Failure

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
CRT with triple site ventricular stimulation
Conventional cardiac resynchronization
Sponsored by
Medtronic Cardiac Rhythm and Heart Failure
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Heart failure, Cardiac resynchronization, Triple site ventricular pacing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Signed informed consent
  • > 18 years old
  • Cardiac resynchronization indication : New York Heart Association (NYHA) Class III/IV & QRS width > 120 ms milliseconds (ms) OR NYHA class II & QRS width > 150 ms
  • Sinus rhythm
  • First implant procedure

Exclusion Criteria:

  • Permanent ventricular tachycardia
  • Permanent pacing indication for 3rd degree atrioventricular (AV) block
  • Diagnosed or suspected acute myocarditis
  • Less than 1 year life expectancy related to a non-cardiovascular disease
  • Impossibility to perform follow-up in the investigative center
  • Pregnant woman
  • Patient which may not cooperate to study procedures as evaluated by investigator
  • Legally protected adult patient or patient unable to give an informed consent
  • Patient enrolled in an other clinical trial
  • Patient which does not benefit from a social protection system
  • Renal insufficiency
  • Patient registered on a heart transplant waiting list
  • Disease and/or health condition which may interfere with study results

Sites / Locations

  • Hôpital Saint Louis
  • University hospital of Bordeaux
  • University hospital of Lille
  • University hospital La Timone
  • University hospital of Montpellier
  • University hospital of Nancy
  • Nouvelles Cliniques Nantaises
  • University hospital of Nantes
  • Clinique Bizet
  • University Hospital of Rennes
  • University hospital of Rouen
  • Centre Cardiologique du Nord

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TRIV

BIV

Arm Description

Cardiac resynchronization with triple site ventricular stimulation (2 RV leads and 1 LV lead)

Conventional cardiac resynchronization

Outcomes

Primary Outcome Measures

Safety of triple site CRT compared to conventional CRT

Secondary Outcome Measures

Feasibility of triple site CRT
Left ventricle remodeling
LV ejection fraction
Cardiac dyssynchrony
Functional status (clinical composite score and NYHA class)
Exercise capacity (6 minutes hall walk test distance)
Quality of life
B-Type Natriuretic Peptide (BNP) level

Full Information

First Posted
April 22, 2009
Last Updated
July 3, 2013
Sponsor
Medtronic Cardiac Rhythm and Heart Failure
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1. Study Identification

Unique Protocol Identification Number
NCT00887237
Brief Title
Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT) Candidates
Acronym
TRIV
Official Title
Triple Site Ventricular Stimulation for CRT Candidates
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Completed
Study Start Date
May 2009 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medtronic Cardiac Rhythm and Heart Failure

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite technological progresses the rate of non-responders to cardiac resynchronization therapy (CRT) remains close to 30%. This inconsistent effect of CRT might be due to incomplete resynchronization as dyssynchrony can persist in 25% to 30% of patients during CRT. One might hypothesize that stimulating the ventricles at a single site is suboptimal and that stimulating multiple left ventricular (LV) or right ventricular (RV) sites may improve ventricular resynchronization and, consequently, its hemodynamic and clinical effects. First studies have suggested that 1 RV + 2 LV pacing sites configurations increased significantly dP/dt, pulse pressure, LV end-diastolic pressure, and is associated with more LV remodeling and better responder rate compared with pacing a single LV site. First studies with 2 RV+LV pacing sites configuration demonstrated increased dP/dt and cardiac output and a decrease of the cardiac dyssynchrony. The present pilot trial was designed to examine the 6-month safety of biventricular stimulation with 2 right ventricular (RV) and 1 left ventricular (LV) leads - main objective- and to assess its clinical benefit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart failure, Cardiac resynchronization, Triple site ventricular pacing

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
76 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TRIV
Arm Type
Experimental
Arm Description
Cardiac resynchronization with triple site ventricular stimulation (2 RV leads and 1 LV lead)
Arm Title
BIV
Arm Type
Active Comparator
Arm Description
Conventional cardiac resynchronization
Intervention Type
Device
Intervention Name(s)
CRT with triple site ventricular stimulation
Intervention Description
CRT with triple site ventricular stimulation (2 RV leads and 1 LV lead)
Intervention Type
Device
Intervention Name(s)
Conventional cardiac resynchronization
Intervention Description
Conventional cardiac resynchronization
Primary Outcome Measure Information:
Title
Safety of triple site CRT compared to conventional CRT
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Feasibility of triple site CRT
Time Frame
6 months
Title
Left ventricle remodeling
Time Frame
At 3 and 6 months
Title
LV ejection fraction
Time Frame
At 3 and 6 months
Title
Cardiac dyssynchrony
Time Frame
At 3 and 6 months
Title
Functional status (clinical composite score and NYHA class)
Time Frame
At 3 and 6 months
Title
Exercise capacity (6 minutes hall walk test distance)
Time Frame
At 3 and 6 months
Title
Quality of life
Time Frame
At 3 and 6 months
Title
B-Type Natriuretic Peptide (BNP) level
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed informed consent > 18 years old Cardiac resynchronization indication : New York Heart Association (NYHA) Class III/IV & QRS width > 120 ms milliseconds (ms) OR NYHA class II & QRS width > 150 ms Sinus rhythm First implant procedure Exclusion Criteria: Permanent ventricular tachycardia Permanent pacing indication for 3rd degree atrioventricular (AV) block Diagnosed or suspected acute myocarditis Less than 1 year life expectancy related to a non-cardiovascular disease Impossibility to perform follow-up in the investigative center Pregnant woman Patient which may not cooperate to study procedures as evaluated by investigator Legally protected adult patient or patient unable to give an informed consent Patient enrolled in an other clinical trial Patient which does not benefit from a social protection system Renal insufficiency Patient registered on a heart transplant waiting list Disease and/or health condition which may interfere with study results
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederic Anselme, Pr
Organizational Affiliation
University Hospital, Rouen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Saint Louis
City
La Rochelle
State/Province
Ile de France
ZIP/Postal Code
17000
Country
France
Facility Name
University hospital of Bordeaux
City
Bordeaux
ZIP/Postal Code
33000
Country
France
Facility Name
University hospital of Lille
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
University hospital La Timone
City
Marseille
ZIP/Postal Code
13000
Country
France
Facility Name
University hospital of Montpellier
City
Montpellier
ZIP/Postal Code
34000
Country
France
Facility Name
University hospital of Nancy
City
Nancy
ZIP/Postal Code
54000
Country
France
Facility Name
Nouvelles Cliniques Nantaises
City
Nantes
ZIP/Postal Code
44000
Country
France
Facility Name
University hospital of Nantes
City
Nantes
ZIP/Postal Code
44000
Country
France
Facility Name
Clinique Bizet
City
Paris
ZIP/Postal Code
75016
Country
France
Facility Name
University Hospital of Rennes
City
Rennes
ZIP/Postal Code
35000
Country
France
Facility Name
University hospital of Rouen
City
Rouen
ZIP/Postal Code
76031
Country
France
Facility Name
Centre Cardiologique du Nord
City
Saint Denis
ZIP/Postal Code
93200
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
26325531
Citation
Anselme F, Bordachar P, Pasquie JL, Klug D, Leclercq C, Milhem A, Alonso C, Deharo JC, Gras D, Probst V, Piot O, Savoure A. Safety, feasibility, and outcome results of cardiac resynchronization with triple-site ventricular stimulation compared to conventional cardiac resynchronization. Heart Rhythm. 2016 Jan;13(1):183-9. doi: 10.1016/j.hrthm.2015.08.036. Epub 2015 Sep 26.
Results Reference
derived

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Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT) Candidates

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