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NCT05646251Completed

Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch Area Pacing (LBBAP)

Intra-procedural Transthoracic EChocardiogram to Facilitate LBBAP

Source: ClinicalTrials.gov · Last updated 1 Oct 2025

Brief summary (registry, in English)

The goal of this observational study is to learn more about whether or not the use of heart ultrasound during pacemaker implantation is helpful. The main questions this aims to answer are: 1. Does this help the doctors with figuring out the wire location during implantation? 2. Does this reduce the wire placement procedure time? 3. Does this reduce the x-ray imaging time during the procedure? Participants will be asked to: 1. Have a physical exam and Echocardiogram (ECG) at initial visit, 2 weeks post implant, and 3 months post implant. 2. Have a urine pregnancy test (if applicable) 3. Have a heart ultrasound during implant procedure 4. Answer questions related to heart failure symptoms to see what stage of heart failure is present 5. Have device interrogation (a wand placed over the chest to see that the device is working properly) at a visit 2 weeks post implant and at 3 months post implant.

Status (registry)
Completed
Study type
Interventional
Enrollment
33 (actual)
First submitted
2 Dec 2022
Start date
1 Mar 2023
Primary completion date
24 Jun 2024
Lead sponsor
Geisinger Clinic
NCT number
NCT05646251

What you commit to

  • Study type: Interventional
  • Participants enrolled: 33
  • From 1 Mar 2023 to the primary completion date, 24 Jun 2024
  • 1 site 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

  • enrolled in a concurrent study that may confound the results of this study

Other

  • Inability to provide informed consent
  • pregnant

Who the study is looking for

  • patient with indication for permanent pacemaker or Implantable Cardioverter Defibrillator (ICD) utilizing conduction system pacing lead for bradycardia or cardiac resynchronization therapy
  • patient is willing to comply with all study procedures and be available for the duration of the study

Age in the registry: 18 years to 89 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Geisinger Clinic
Coordinator of this site? Confirm its status
Wilkes-BarreUnited StatesUnknown status

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