Clinical Trials Logo

Clinical Trial Summary

This study is a multi-center open-label randomized study, and we sought to investigate the redundancy of post-procedural prophylactic antibiotics in cardiac implantable electronic device implantation. There are 2 arms in this study. One arm will receive pre-procedural intravenous antibiotics only. The other arm will receive both pre-procedural intravenous antibiotics and post-procedural 3-day oral antibiotics.


Clinical Trial Description

There is general agreement on the benefits of preoperative prophylactic antibiotics which had been documented in previous studies. Concerns of bacterial resistance and unnecessary cost, our prospective observational case-control study had suggested the redundancy of post-procedural antibiotics. In this well-designed study, we sought to investigate the efficacy of post-procedural antibiotics and confirm the hypothesis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04146883
Study type Interventional
Source National Cheng-Kung University Hospital
Contact Hui-Chen Chiang, Bachelor
Phone +886-6-2353535
Email atiffany543783@gmail.com
Status Recruiting
Phase N/A
Start date August 20, 2019
Completion date December 31, 2021

See also
  Status Clinical Trial Phase
Terminated NCT02243696 - Protego DF4 Post Approval Registry
Completed NCT02902458 - Psychological Intervention modifiEs Outcome of Patients With implAntable Cardioverter dEfibrillator: The PEACE Study N/A
Recruiting NCT02058771 - Utilising Lifemap to Investigate Malignant Arrhythmia Therapy
Completed NCT02232204 - Sleep and Ventricular Arrhythmias Study Phase 2
Recruiting NCT05302115 - S-ICD French Cohort Study (HONEST)
Completed NCT05101720 - Ultrasound Guided Axillary Access vs Standard Fluoroscopic Technique for Cardiac Lead Implantation: ZEROFLUOROAXI TRIAL N/A
Active, not recruiting NCT03884608 - Analysis of Both Sex and Device Specific Factors on Outcomes in Patients With Non-Ischemic Cardiomyopathy
Completed NCT02787291 - A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse VR ICD Undergoing MRI, an IDE Study N/A
Completed NCT02064192 - Comparative Effectiveness Research to Assess the Use of Primary ProphylacTic Implantable Cardioverter Defibrillators in Europe
Terminated NCT03103503 - Plexa ICD Lead Registry
Recruiting NCT05855135 - Assessment of Combined CCM and ICD Device in HFrEF N/A
Recruiting NCT04858672 - Shock Testing to Unmask RV Lead and GEnerator Malfunction in ICD Patients: the SURGE-ICD Registry
Completed NCT03209726 - Assessment of S-ICD Eligibility With 12-Lead ECG
Active, not recruiting NCT04981496 - Novel ICD Arrhythmia Detection Algorithm
Recruiting NCT05645965 - Association of Obesity and Cardiovascular Outcomes in Patients With Implantable Cardioverter-defibrillator (ICD)
Completed NCT03544489 - Implementing Exercise After an (ICD) N/A
Completed NCT03210883 - Global Electrical Heterogeneity and Clinical Outcomes
Completed NCT02491853 - The Gulf Implantable Cardioverter-Defibrillator Registry N/A
Completed NCT01944514 - Implantable Cardioverter Defibrillators - Improving Risk Stratification N/A
Completed NCT04994782 - GAMification to Encourage End-Of-Life Discussions Between ICD Patients and Caregivers N/A