CS-03 Pressure-Volume Loop Sub-study With RV Lead Positioning
Primary Purpose
Hypertension
Status
Active
Phase
Not Applicable
Locations
Czechia
Study Type
Interventional
Intervention
BackBeat-PHC
Sponsored by

About this trial
This is an interventional basic science trial for Hypertension
Eligibility Criteria
Inclusion Criteria:
- Subject was included in the CS-03 study
- Subject indicated for a de novo pulse generator implant
Exclusion Criteria:
- Subject was excluded from the CS-03 study
- Subject is not 100% dependent on RV pacing
- Subject receiving a pacemaker pulse generator exchange
- Subject is unwilling or cannot provide Informed Consent for this sub study
Sites / Locations
- Na Homolce Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
RV location
Arm Description
All included subjects will undergo the PV loop test with 'BackBeat PHC' ON and OFF
Outcomes
Primary Outcome Measures
Change in the LV volumes (ml)
LV volume will be assessed in two RV electrode lead locations with BackBeat PHC ON and OFF
Change in the LV pressures (mmHg)
LV pressure will be assessed in two RV electrode lead locations with BackBeat PHC ON and OFF
Secondary Outcome Measures
Change in the pressure-volume ratio
LV pressure will be assessed in two RV electrode lead locations with BackBeat PHC ON and OFF
Full Information
NCT ID
NCT02909868
First Posted
September 13, 2016
Last Updated
January 9, 2023
Sponsor
BackBeat Medical Inc
1. Study Identification
Unique Protocol Identification Number
NCT02909868
Brief Title
CS-03 Pressure-Volume Loop Sub-study With RV Lead Positioning
Official Title
Clinical Evaluation of Safety and Effectiveness of the BackBeat Medical Moderato System in Patients With Hypertension: A Double-Blind Randomized Trial - PV Loops Sub-study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 15, 2016 (Actual)
Primary Completion Date
August 1, 2021 (Actual)
Study Completion Date
September 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
BackBeat Medical Inc
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The position of the RV lead may have an important role in the effectiveness of the Programmable Hypertension Control (PHC) therapy by the Moderato pacemaker eliciting a lag from which RV signals (QRS) are identified.
The study attempts to measure RV Pressure and RV Volume with PHC in two RV lead locations.
Detailed Description
Subjects found eligible for participation in the CS-03 study, who are indicated for a de novo pulse generator implant at the center participating in this sub-study and who are not 100% dependent on RV pacing are eligible for participation in this sub-study.
Patients receiving a pacemaker pulse generator exchange or who are 100% pacemaker dependent may not participate.
Eligible patients will be provided with an Informed Consent specific to this sub-study and if patients choose to participate, patients will be asked to sign the Informed Consent and will then undergo the procedures described below.
Patients will be prepared and draped for the Moderato implant procedure as detailed in the main CS-03 study protocol.
Subjects will be instrumented prior to the Moderato Pacemaker implant procedure.
The position of the RV lead will be tested at two sites known to elicit shortest QRS duration (The RV apical septum and the His region).
A series of three test periods with the Moderato System programmed to deliver predetermined PHC settings will follow.
Following the completion of these measurements, the conductance catheter will be withdrawn and the Moderato System implant will resume as described in the CS-03 protocol.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
RV location
Arm Type
Experimental
Arm Description
All included subjects will undergo the PV loop test with 'BackBeat PHC' ON and OFF
Intervention Type
Device
Intervention Name(s)
BackBeat-PHC
Intervention Description
A conductance catheter will be used to obtain PV loops prior to a Moderato pacemaker implant procedure.
Primary Outcome Measure Information:
Title
Change in the LV volumes (ml)
Description
LV volume will be assessed in two RV electrode lead locations with BackBeat PHC ON and OFF
Time Frame
up to 2 hr
Title
Change in the LV pressures (mmHg)
Description
LV pressure will be assessed in two RV electrode lead locations with BackBeat PHC ON and OFF
Time Frame
up to 2 hr
Secondary Outcome Measure Information:
Title
Change in the pressure-volume ratio
Description
LV pressure will be assessed in two RV electrode lead locations with BackBeat PHC ON and OFF
Time Frame
up to 2 hr
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subject was included in the CS-03 study
Subject indicated for a de novo pulse generator implant
Exclusion Criteria:
Subject was excluded from the CS-03 study
Subject is not 100% dependent on RV pacing
Subject receiving a pacemaker pulse generator exchange
Subject is unwilling or cannot provide Informed Consent for this sub study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Petr Neuzil, Prof.
Organizational Affiliation
Na Homolce Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Na Homolce Hospital
City
Prague
Country
Czechia
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
11738311
Citation
Chen CH, Fetics B, Nevo E, Rochitte CE, Chiou KR, Ding PA, Kawaguchi M, Kass DA. Noninvasive single-beat determination of left ventricular end-systolic elastance in humans. J Am Coll Cardiol. 2001 Dec;38(7):2028-34. doi: 10.1016/s0735-1097(01)01651-5.
Results Reference
background
PubMed Identifier
17853871
Citation
Klotz S, Dickstein ML, Burkhoff D. A computational method of prediction of the end-diastolic pressure-volume relationship by single beat. Nat Protoc. 2007;2(9):2152-8. doi: 10.1038/nprot.2007.270.
Results Reference
background
Learn more about this trial
CS-03 Pressure-Volume Loop Sub-study With RV Lead Positioning
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