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Prospective Multicentric Study Comparing the Acute Hemodynamic Effect of Three Modes of Stimulation in Cardiac Resynchronization Therapy Recipients (3 STIM)

Primary Purpose

Heart Failure, Cardiac Resynchronization Therapy

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Device programming of ABBOTT CRT pacemaker or defibrillator
Sponsored by
CMC Ambroise Paré
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Cardiac Resynchronization Therapy, Atrioventricular delay optimization, Multipoint pacing, Negative atrioventricular hysteresis, Non invasive hemodynamic optimization, Heart Failure

Eligibility Criteria

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

Inclusion Criteria:

  • Patient older than 18
  • Implantation of a CRT (CRT-P or CRT-D) less than 3 months before inclusion
  • MPP and SyncAV-enabled ABBOTT Quadripolar CRT pacing system
  • Patient who had signed an informed consent and is willing to comply with study requirements
  • De novo implantation
  • Patient covered by national healthcare insurance

Exclusion Criteria:

  • Permanent/persistant atrial fibrillation/ supra-ventricular tachycardia
  • Pacing indication for 2nd or 3rd degree AV block
  • Upgrading from non-CRT system
  • Pregnant or breastfeeding women
  • Adult under legal protection

Sites / Locations

  • Gehm Site D'Eaubonne
  • Cmc Ambroise Pare
  • CHU Poitiers

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CRT device

Arm Description

Patients implanted with a CRT device who will undergo a non-invasive hemodynamic evaluation of different pacing modes

Outcomes

Primary Outcome Measures

Hemodynamic response
Highest Systolic Blood Pressure (SBP) obtained by optimization of the mode of stimulation

Secondary Outcome Measures

Other hemodynamical response
Cardiac output
Other hemodynamical response
Systolic ejection volume
Other hemodynamical response
dP/dT

Full Information

First Posted
December 17, 2018
Last Updated
May 20, 2020
Sponsor
CMC Ambroise Paré
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1. Study Identification

Unique Protocol Identification Number
NCT03779802
Brief Title
Prospective Multicentric Study Comparing the Acute Hemodynamic Effect of Three Modes of Stimulation in Cardiac Resynchronization Therapy Recipients
Acronym
3 STIM
Official Title
Comparison of the Acute Hemodynamic Effect of Three Modes of Stimulation in Cardiac Resynchronization.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Terminated
Why Stopped
With the current health situation, we do not anticipate a significant resumption of recruitment for several months.
Study Start Date
April 23, 2019 (Actual)
Primary Completion Date
April 18, 2020 (Actual)
Study Completion Date
April 18, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CMC Ambroise Paré

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Cardiac Resynchronization Therapy (CRT) is an established treatment for patients with systolic heart failure and bundle branch block, improving functional capacity, quality of life and reducing morbi-mortality. Adjusting atrio-ventricular (AV) delay, vector optimization and choice of different modes of stimulation can influence the acute hemodynamical consequences of CRT but also its medium-term and long-term clinical and echocardiographic effects. The aim of the present prospective study is to investigate whether the different stimulation modes lead to different acute hemodynamic response, by evaluating the highest systolic pressure using the Finapress ® method.
Detailed Description
This study is a non-randomized, prospective, interventional, multicentric study. Patients implanted with an Abbott ® CRT pacemaker or defibrillator since less than 3 months are eligible for the study. Recruited patients will be submitted to a non-invasive evaluation of different pacing modes. This will be performed using the Finapress NOVA device, which records blood pressure with a digital cuff. The peak of blood pressure will correspond to the optimal device settings Three modes of stimulation of ABBOTT CRT devices will be compared: Classical bi-ventricular pacing mode at nominal value and with AV delay optimization SyncAV mode at nominal value or with left ventricular preexcitation optimization Multipoint Pacing (MPP) mode, alone or in combination with SyncAV mode This is an acute evaluation study without scheduled follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Cardiac Resynchronization Therapy
Keywords
Cardiac Resynchronization Therapy, Atrioventricular delay optimization, Multipoint pacing, Negative atrioventricular hysteresis, Non invasive hemodynamic optimization, Heart Failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CRT device
Arm Type
Experimental
Arm Description
Patients implanted with a CRT device who will undergo a non-invasive hemodynamic evaluation of different pacing modes
Intervention Type
Other
Intervention Name(s)
Device programming of ABBOTT CRT pacemaker or defibrillator
Intervention Description
Comparison of the acute hemodynamic effect of three modes of stimulation in ABBOTT CRT devices (Biventricular, SyncAV and MPP modes) by using the Finapress® NOVA method to assess the highest systolic blood pressure (SBP) during the programming session Comparison of the acute hemodynamic effect of three modes of stimulation in ABBOTT CRT devices (Biventricular, SyncAV and MPP modes) by using the Finapress® NOVA method to assess the highest systolic blood pressure (SBP) during the programming session.
Primary Outcome Measure Information:
Title
Hemodynamic response
Description
Highest Systolic Blood Pressure (SBP) obtained by optimization of the mode of stimulation
Time Frame
day 0
Secondary Outcome Measure Information:
Title
Other hemodynamical response
Description
Cardiac output
Time Frame
day 0
Title
Other hemodynamical response
Description
Systolic ejection volume
Time Frame
day 0
Title
Other hemodynamical response
Description
dP/dT
Time Frame
day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient older than 18 Implantation of a CRT (CRT-P or CRT-D) less than 3 months before inclusion MPP and SyncAV-enabled ABBOTT Quadripolar CRT pacing system Patient who had signed an informed consent and is willing to comply with study requirements De novo implantation Patient covered by national healthcare insurance Exclusion Criteria: Permanent/persistant atrial fibrillation/ supra-ventricular tachycardia Pacing indication for 2nd or 3rd degree AV block Upgrading from non-CRT system Pregnant or breastfeeding women Adult under legal protection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ghassan MD MOUBARAK
Organizational Affiliation
CMC Ambroise Paré
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gehm Site D'Eaubonne
City
Eaubonne
State/Province
Val-d'Oise
ZIP/Postal Code
95600
Country
France
Facility Name
Cmc Ambroise Pare
City
Neuilly sur seine
ZIP/Postal Code
92200
Country
France
Facility Name
CHU Poitiers
City
Poitiers
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33128179
Citation
Ferchaud V, Garcia R, Bidegain N, Degand B, Milliez P, Pezel T, Moubarak G. Non-invasive hemodynamic determination of patient-specific optimal pacing mode in cardiac resynchronization therapy. J Interv Card Electrophysiol. 2021 Nov;62(2):347-356. doi: 10.1007/s10840-020-00908-6. Epub 2020 Oct 30.
Results Reference
derived

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Prospective Multicentric Study Comparing the Acute Hemodynamic Effect of Three Modes of Stimulation in Cardiac Resynchronization Therapy Recipients

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