Left Bundle Branch Area Pacing Clinical Trials
2 recruiting trials for Left Bundle Branch Area Pacing. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Left Bundle Branch Area Pacing clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Yonsei University (1), Abbott Medical Devices (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is Left bundle branch area pacing (procedure, 1 trial), followed by Right ventricular pacing, LBBAP lead.
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Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
PReventive Effect Of Left Bundle Branch Area Pacing Versus righT vEntricular paCing on All Cause deaTh, Heart Failure...
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...
Left Bundle Branch Area Pacing (LBBAP) PMCF Study
The objective of this study is to evaluate the safety and effectiveness of LBBA pacing/sensing in patients implanted with the Tendril STS 2088TC or UltiPace LPA1231 lead through 6...
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Frequently Asked Questions
There are currently 2 clinical trials for Left Bundle Branch Area Pacing, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Left Bundle Branch Area Pacing, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Left Bundle Branch Area Pacing, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.