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
- Diseases
- Heart failure
- 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
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Geisinger Clinic Coordinator of this site? Confirm its status | Wilkes-Barre | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.