About this trial
This prospective observational cohort study will evaluate the extent to which cardiac implantable electronic device (CIED) implantation techniques at Assiut University Heart Hospital (AUHH) align with the evidence-based recommendations of the European Society of Cardiology (ESC).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All addult patients (≥18 years) referred foran indicatedCIED implantation at Assiut University Heart Hospital
Disqualifiers
Previous implantation of CIED implantation
General contraindications of CIED
Patient refusal
Trial population
Study will involve adult patients (≥18 years) receiving CIED for standard arrhythmic, conduction system diseases or heart failure indications over a period of two years,
Trial design
Cohort
Prospective
Treatments tested in this trial
CIEDimplantation
DeviceCompare current procedural CIED practice at AUHH to recent ESC guidelines.
Treatment groups
Trial outcomes
Primary outcomes
Incidence of procedure-related early complications (composite)
Percentage of patients who develop any of the following within 30 days after pacemaker implantation: hematoma requiring intervention, lead dislodgement requiring reintervention, pneumothorax requiring treatment, pocket or device-related infection requiring antibiotics or device removal, acute pacing failure or sensing abnormality requiring reintervention
Secondary outcomes
Incidence of late complications after pacemaker implantation
Number and percentage of patients who develop late device-related complications such as pocket erosion, late infection, venous thrombosis, or lead malfunction after 30 days and up to 12 months post-implantation.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: