The Fluoroless-CSP Trial Using Electroanatomic Mapping

Not Applicable

• Conditions: Sinus Node Dysfunction; Heart Block AV; LBBB; Heart Failure, Systolic

• Registration Number: NCT03903107
• Lead Sponsor: Rush University Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-10-31
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Inclusion Criteria:<br><br> - Age > 18 years<br><br> - Indication for Permanent Pacemaker implantation or implantation of Cardiac<br> Resynchronization Therapy Device<br><br>Exclusion Criteria:<br><br> - Existing cardiac device including Pacemaker or Cardiac Resynchronization Therapy<br> device<br><br> - Inability of patient capacity to provide consent for themselves either due to<br> medical or psychiatric comorbidity<br><br> - Pregnancy<br><br> - Difficulty with follow-up

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Success of achieving CSP

Secondary Outcome Measures

Name	Time	Method
Total radiation exposure time during procedure;Procedure-related complications;Need for His Lead revisions