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OPTImizing Lead Placement in Patients Requiring Pacemaker After Cardiac Surgery (OPTI-PACS)

26. august 2026 opdateret af: Andreas Martinsson, Sahlgrenska University Hospital

OPTIMIZING LEAD PLACEMENT IN PATIENTS REQUIRING PACEMAKER AFTER CARDIAC SURGERY

Conventional right ventricular pacing has been associated with ventricular dyssynchrony and an increased risk of pacing-induced cardiomyopathy, which may lead to worse clinical outcomes. To lessen the burden of pacing-induced cardiomyopathy, the adoption of conduction system pacing has increased in recent years. In patients with normal cardiac function, measured as left ventricular ejection fraction, the superiority of conduction system pacing is less clear. As a result, both pacing strategies remain in widespread clinical use.

Patients undergoing cardiac surgery represent a vulnerable cohort for pacing-induced cardiomyopathy, given their established structural heart disease, and postoperative atrioventricular block remains a common occurrence in these patients.

This multicenter randomized trial aims to evaluate the use of conduction system pacing, in the form of left bundle branch area pacing, versus conventional pacing in patients with normal left ventricular ejection fraction after cardiac surgery.

Studieoversigt

Detaljeret beskrivelse

A high percentage of ventricular pacing increases the risk of pacing-induced cardiomyopathy. Pacing-induced cardiomyopathy is a syndrome defined by left ventricular dysfunction secondary to chronic right ventricular pacing, resulting in impaired outcomes. Pacing-induced cardiomyopathy is estimated to affect approximately 10-20% of patients with a high proportion of right ventricular pacing (>20%), a population that mainly consists of patients with atrioventricular block (AVB). The abnormal activation leads to prolonged electrical and mechanical activation, which results in ventricular dyssynchrony. Other important risk factors for pacing-induced cardiomyopathy include structural heart disease and reduced ejection fraction, male sex and wide, paced QRS.

Clinical practice guidelines support pacemaker implantation following cardiac surgery only for severe and non-transient bradyarrhythmias, as pacemaker implantation increases the risk of severe infections and device-related long-term complications. Evidence suggests that a substantial proportion of patients who receive a pacemaker following cardiac surgery have limited need for pacing at long-term follow-up. Thus, the risk/benefit ratio for patients following cardiac surgery differs from that of the general population, while these patients also form a vulnerable population at high risk for pacing-induced cardiomyopathy.

Over the last decade, a conduction system pacing strategy called left bundle branch area pacing (LBBAP) has been developed. In LBBAP, the pacemaker lead is inserted deep into the interventricular septum from the right ventricle to the left ventricular endocardium, targeting the left bundle and its resulting fascicles. As the current understanding of the development of pacing-induced cardiomyopathy suggests that the electrical dyssynchrony introduced by right ventricular pacing plays a crucial role, our hypothesis is that its incidence could be reduced by the favorable electrical activation achieved with LBBAP.

There are ongoing randomized controlled trials of conduction system pacing in the general population; however, none are investigating cardiac surgery patients. These patients differ substantially from the general population in age, expected long-term survival, and cardiovascular health. This increases their risk of pacing-induced cardiomyopathy and could influence the feasibility of conduction system pacing due to their otherwise impaired cardiovascular health. At the same time, their long-term pacing dependence could differ from that of the general population.

Therefore, the aim of the present multicenter randomized controlled trial is to evaluate the long-term outcomes of LBBAP versus right ventricular pacing after cardiac surgery in patients with normal left ventricular ejection fraction. A secondary aim is to assess the feasibility of LBBAP after cardiac surgery with regard to implantation success and long-term electrical parameters. The results of this trial are anticipated to provide clinically meaningful evidence to guide pacing strategy selection in this patient cohort.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

110

Fase

  • Ikke anvendelig

Kontakter og lokationer

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Deltagelseskriterier

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Beskrivelse

Inclusion Criteria:

  • High degree atrioventricular block
  • Cardiac surgery within 30 days of pacemaker implantation
  • Written informed consent
  • Current left ventricular ejection fraction at or above 50%

Exclusion Criteria:

  • Any concomitant condition that results in a life expectancy of less than 1 year
  • Planned for heart transplant or left ventricular assist device
  • Current dialysis
  • Not suitable according to the opinion of the investigators due to characteristics that interfere with the adherence to the study protocol.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Conventional pacing strategy
This arm will receive a conventional pacemaker lead if they have atrioventricular block after cardiac surgery
Conventional pacing strategy
Eksperimentel: Left bundle branch area pacing strategy
This arm will receive a left bundle branch area pacing pacemaker lead if they have atrioventricular block after cardiac surgery
Conventional pacing strategy versus conduction system pacing strategy in the form of left bundle branch area pacing

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in left ventricular ejection fraction
Tidsramme: 1 year
Change in left ventricular ejection fraction between enrollment and end of follow-up
1 year

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Dødelighed af alle årsager
Tidsramme: 1 år
Dødelighed af alle årsager
1 år
Change in left ventricular end-diastolic diameter
Tidsramme: 1 year
Change in LVEDD from enrollment to end of study follow-up
1 year
Clinical endpoints - composite
Tidsramme: 1 year
Composite of all-cause mortality, heart failure hospitalization, device-related hospitalization
1 year
Heart failure hospitalization
Tidsramme: 1 year
Heart failure hospitalization
1 year
Device-related hospitalization
Tidsramme: 1 year
Device-related hospitalization
1 year
Quality-of-life measurement
Tidsramme: 1 year
Quality-of-life measurement by standardized questionnaire
1 year

Samarbejdspartnere og efterforskere

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Efterforskere

  • Ledende efterforsker: Andreas S Martinsson, MD, PhD, Sahlgrensa university hospital

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

10. september 2026

Primær færdiggørelse (Anslået)

1. december 2030

Studieafslutning (Anslået)

1. december 2030

Datoer for studieregistrering

Først indsendt

26. august 2026

Først indsendt, der opfyldte QC-kriterier

26. august 2026

Først opslået (Faktiske)

31. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

31. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

26. august 2026

Sidst verificeret

1. august 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2025-08652-01
  • 2025 (U.S. NIH-bevilling/kontrakt: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • 20241208 (Andet bevillings-/finansieringsnummer: Swedish Heart- Lung Foundation)
  • ALFGBG-977905 (Andet bevillings-/finansieringsnummer: ALF Agreement (Swedish state))
  • ALFGBG-1029431 (Andet bevillings-/finansieringsnummer: ALF Agreement (Swedish state))

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