Safe Traction During Ongoing Lead Extraction Procedure (STOP)
Completed
- Conditions
- Infections of Cardiac Electronic Implantable DevicesElectrode Malfunction
- Registration Number
- NCT01847625
- Lead Sponsor
- Deutsches Herzzentrum Muenchen
- Brief Summary
The study will evaluate (in-vitro) the forces that are typically used for the extraction of pacemaker or defibrillator electrodes.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Experience in pacemaker and defibrillator lead extraction
Exclusion Criteria
- none
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Forces used for lead extraction 10 Minutes
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms are involved in cardiac lead extraction force measurement techniques?
How does the STOP trial compare to standard-of-care methods for managing electrode malfunction in cardiac devices?
Are there specific biomarkers that indicate higher risk for complications during lead extraction procedures?
What are the potential adverse events associated with in-vitro lead extraction force evaluation methods?
What alternative or combination approaches are being explored for extracting infected cardiac electronic implants?
Trial Locations
- Locations (1)
Deutsches Herzzentrum München
🇩🇪Munich, Bayern, Germany
Deutsches Herzzentrum München🇩🇪Munich, Bayern, Germany