Samsung Medical Center
Seoul, 06351, South Korea
Location status: Recruiting
NCT Number: NCT07563153
This study aims to evaluate the clinical impact of an optimized pacing strategy in patients with heart failure.
* Intervention: Adjustment of the pacemaker lower rate limit to an individualized, hemodynamically optimized heart rate. * Primary Endpoint: Heart failure symptoms, assessed by the Kansas City Cardiomyopathy Questionnaire score. * Hypothesis: In patients with heart failure requiring permanent pacing, an optimized pacing strategy will lead to a significant improvement in heart failure symptoms (Kansas City Cardiomyopathy Questionnaire score) at 12 months compared with the conventional pacing strategy.
Interested in participating?
Request Info19 year and older
All sexes
Interventional
Not applicable
Seoul, 06351, South Korea
Location status: Recruiting
Heart failure is a growing health concern with increasing prevalence in the aging population, and permanent pacemaker implantation is frequently required due to concomitant bradyarrhythmias. Heart rate is closely associated with hemodynamic status in patients with heart failure; however, evidence guiding the optimal pacemaker lower rate setting remains limited. Although the conventional lower rate is typically set at 50-60 bpm, recent studies suggest that a moderately increased pacing rate may improve hemodynamics and clinical outcomes. Furthermore, advances in physiological pacing techniques, such as conduction system pacing, provide the potential for greater clinical benefits through optimized heart rate settings in this patient population.
Enrolled subjects are randomized in a 1:1 ratio into either the optimized pacing group or the conventional pacing strategy group based on stratification factors.
The optimized pacing group undergoes post-procedural right heart catheterization with adjustments to the lower rate limit, where the heart rate (HR) that yields the lowest mean pulmonary capillary wedge pressure (mPCWP) or the highest cardiac output is determined as the optimal HR. In the conventional pacing strategy group, the lower rate limit is set at 60 bpm. Clinical symptoms and parameters of both groups are subsequently compared over a one-year follow-up period.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
(Sufficient cardiac physiologic pacing is defined as a paced QRS duration ≤ 140 ms.)
Optimized Pacing Strategy
Conventional Pacing Strategy
Time frame: From enrollment to 1year after the procedure
Higher scores indicate better health status and a higher quality of life, score 0 to 100
Time frame: From enrollment to 1year after the procedure
pg/mL (picograms per milliliter)
Time frame: From enrollment to 1year after the procedure
class I to IV, higher NYHA classes indicate poorer functional status.
Time frame: From enrollment to 1year after the procedure
m
Time frame: From enrollment to 1year after the procedure
Documented incidence of atrial fibrillation on 12-lead ECG
Time frame: From enrollment to 1year after the procedure
Atrial fibrillation burden(%) recorded by CIEDs
Time frame: At the time of CIED implantation
pressure of RA, RV, PA, PCWP as mmHg Cardiac output as L/min (Liters per minute)
Time frame: From enrollment to 1year after the procedure
year
Time frame: From enrollment to 1year after the procedure
All-cause mortality rate(%) during 1year follow-up
Time frame: From enrollment to 1year after the procedure
Cardiac mortality rate(%) during 1year follow-up
Time frame: From enrollment to 1year after the procedure
All cause re-hospitalization rate(%) during 1year follow-up
Time frame: From enrollment to 1year after the procedure
Hospitalization due to heart failure rate(%) during 1year follow-up
Time frame: From enrollment to 1year after the procedure
Average heart rate(bpm) monitored by the device
Time frame: From enrollment to 1year after the procedure
heart rate distribution recorded in CIED (% of total time) 60bpm to 70 70bpm to 80 80bpm to 90 90bpm to 100 over 100bpm
Time frame: From enrollment to 1year after the procedure
Atrial pacing and ventricular pacing burden(%) recorded in CIEDs
Time frame: From enrollment to 1year after the procedure
Peak VO2 and VO2 at AT measured by cardiopulmonary exercise test. Both parameter calculated in mL/kg/min
Time frame: From enrollment to 1year after the procedure
LVEF(%) measured by echocardiogram
Time frame: From enrollment to 1year after the procedure
E/e' ratio, calculated as the ratio of early mitral inflow velocity (E) to early diastolic mitral annular velocity (e'), both velocities measured in m/s.
Time frame: From enrollment to 1year after the procedure
Cardiac index(as L/min/m^2) measured with echocardiogram and body surface area
Time frame: From enrollment to 1year after the procedure
Peak TR velocity(TR V max) measured by echocardiogram (m/s)
Time frame: From enrollment to 1year after the procedure
Left atrial strain(%) measured by echocardiogram
Time frame: From enrollment to 1year after the procedure
QRS duration, QT interval, P wave duration, PR interval (as ms)
Contact information is provided by the study sponsor or research team.
Samsung Medical Center
Other
Clinical and Hemodynamic Outcomes of OPTimized PACing StratEgies in Heart Failure Patients With Pacing Indications: Randomized-Controlled Trial (OPTPACE-HF)
Acronym: OPTPACE-HF
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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