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NCT05585411Recruiting

PReventive Effect Of Left Bundle Branch Area Pacing Versus righT vEntricular paCing on All Cause deaTh, Heart Failure Progression, and Ventricular dysSYNChrony in Patients With Substantial Ventricular Pacing (PROTECT-SYNC): Multicenter Prospective Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 5 Jan 2026

Brief summary (registry, in English)

PROTECT-SYNC study is a multicenter, randomized, controlled trial. A total of 7 medical centers across Republic of Korea will enroll 450 patients during 2 years of enrollment period, and followed for 2 years of follow-up period. The purpose of this study to compare the clinical outcomes of Left Bundle Branch Area Pacing (LBBAP) compared to Right Ventricular Pacing (RVP) in bradyarrhythmia patients who require high burden of ventricular pacing (\>40%).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
450 (estimated)
First submitted
14 Oct 2022
Start date
1 Nov 2022
Primary completion date
1 Nov 2026
Lead sponsor
Yonsei University
NCT number
NCT05585411

What you commit to

  • Study type: Interventional
  • Planned participants: 450
  • From 1 Nov 2022 to the primary completion date, 1 Nov 2026
  • 8 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior myocardial infarction including ventricular septum
  • Prior Heart transplant surgery

Other illness

  • History of prosthetic valve surgery on tricuspid valve
  • Life expectancy \< 12 months due to any condition

Other

  • Incapacitated or unable to read or write
  • Patient who is an indication of ICD or CRT
  • Unavailable for at least 24 months of follow-up visits
  • Pregnant or breastfeeding at the time of signing consent
  • Persistent Left Superior Vena Cava (PLSVC)

Who the study is looking for

  • At least 19 years old and willing and capable to give informed consent
  • Patients who is willing and able to comply with the prescribed follow-up tests and schedule of evaluations.
    • 3 Scheduled to receive a pacemaker implant 4. Substantial percentage of V pacing rate (\>40%) is anticipated

Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bucheon Sejong Hospital
Coordinator of this site? Confirm its status
Bucheon-siSouth KoreaRecruiting
Gyeongsang National University Changwon hospital
Coordinator of this site? Confirm its status
ChangwonSouth KoreaRecruiting
Chungbuk National University Hospital
Coordinator of this site? Confirm its status
ChungjuSouth KoreaRecruiting
Yonsei University Health System, Severance Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaNot yet recruiting
Kyunghee university hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting
Seoul saint Mary's Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting
Asan Medical Center
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting
Seoul National University Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.