SCOPE-CRT: Simultaneous or Sequential Multipoint Pacing
Study Details
Study Description
Brief Summary
The purpose of this study is to compare electrical acute changes between simultaneous and sequential LV pacing and to assess the paced QRSd over a range of inter- and intra-ventricular programmable delays setting during MPP pacing.
| Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
The study will be a prospective, single-arm, non-randomized, non-blinded, acute study conducted at CRT device implant and prior to subject discharge. Subjects scheduled to be implanted with a Quadripolar Pacing System who provide informed consent will undergo "Enrollment" and participate in "SCOPE-CRT" study. Enrollment and device implant can occur in the same day. Including Enrollment, each subject's participation is expected to be 1-2 days. The total duration of the study is expected to be 12 months, including Enrollment. Enrollment will include the Informed Consent process, physical examination, and collection of demographics, cardiovascular history, medical history, and medications.
During CRT implant, surface ECG and PV loop recordings will be taken over the different programmable MPP settings. Following data collection, CRT device programming will be left to the discretion of the physician.
Study Design
Outcome Measures
Primary Outcome Measures
- Acute QRS duration changes during multipoint CRT [1 day during CRT]
Quantify acute changes in surface ECG QRS duration between simultaneous and sequential LV pacing during MPP pacing.
Secondary Outcome Measures
- Acute ECG QRS duration changes during multipoint CRT [1 day during CRT]
Quantify acute changes in surface ECG QRSd over a range of inter- and intra-ventricular programmable delays setting during multipoint CRT pacing. •
- Acute changes in hemodynamics between simultaneous and sequential LV pacing during multipoint CRT [1 day during CRT]
Quantify acute changes in hemodynamics between simultaneous and sequential LV pacing during multipoint CRT pacing over a range of inter- and intra-ventricular programmable delays settings.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patients with approved indication for CRT by European Society of Cardiology/European Heart Rhythm Association guidelines (ESC/EHRA)
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QRS duration > 130 ms
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Ability to provide informed consent for study participation
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At least 18 years of age
Exclusion Criteria:
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Myocardial infarction within 40 days before enrolment
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NYHA Class IV
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Tachyarrhythmia caused by temporary or reversible irritation, e.g. poisoning, electrolyte imbalance, hypoxia, sepsis or acute myocardial infarction
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Such frequent VT or VF that the therapies would cause an unacceptably rapid depletion of the device batteries
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VT with few or without clinically relevant symptoms
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VT or VF treatable by surgery
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Concomitant diseases that would substantially limit a positive prognosis
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Accelerated intrinsic rhythm
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Women who are pregnant
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | IRCCS Policlinico S. Donato | San Donato Milanese | Milano | Italy | 20097 |
Sponsors and Collaborators
- IRCCS Policlinico S. Donato
Investigators
- Principal Investigator: Carlo Pappone, MD, IRCCS San Donato University Hospital Policlinico San Donato, Milan, Italy
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- SCOPE-CRT IRCCSDonato