Randomised study to investigate pain and Patient satisfaction with audiovisual distraction during Pacemaker and ICD-implantatio
Not Applicable
Recruiting
- Conditions
- patients with indication for Implantation of a Pacemaker or ICD
- Registration Number
- DRKS00017420
- Lead Sponsor
- eipzig Heart Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
informed consent
Patient >=18 years old
Implantation, battery Exchange of a Pacemaker or ICD in local anesthesia
Exclusion Criteria
blindness
psychiatric diseases (schizophrenia, dementia, Delir)
injuries of the head which prevent the use of Video glasses
patients with multiresistent germs
pregnant women
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain perception, evaluated with numeric Rating scale at different time Points before, during and after the intervention
- Secondary Outcome Measures
Name Time Method amount of painkillers and sedatives during the procedure<br>Evaluation of patient satisfaction with a numeric Rating scale