Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03114124 · ClinicalTrials.gov registry record · NA

Microfidelity (MIFI) Ablation Technology Versus Standard Ablation Catheter for Atrioventricular Nodal Ablation

A NA study, sponsored by University of Florida.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT03114124: Completed NA study, sponsored by University of Florida.

NCT03114124 is a NA study that has completed, run by University of Florida. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03114124, a NA study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

The aim of our study is to investigate the comparative efficacy of high fidelity multi electrode ablation catheters vs the standard bipolar configuration in success of AV nodal ablation This study will provide insights on the use of new technology where application may increase efficacy, promote patient and physician safety and decrease costs.

Primary Outcome

Identified by a junctional rhythm or complete heart block. Time zero is when the ablation procedure begins and the successful outcomes are either complete heart block or junctional rhythm.

Interventions

  • DEVICE MIFI Catheter
  • DEVICE Standard Ablation Catheter

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2017-05-23
Est. Completion 2019-11-09
Phase NA
University of Florida

1,106 total trials

What the finished NCT03114124 record still lists

NCT03114124 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which MIFI Catheter is the first listed.

NCT03114124 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03114124 about?

NCT03114124 is a clinical study titled "Microfidelity (MIFI) Ablation Technology Versus Standard Ablation Catheter for Atrioventricular Nodal Ablation". The aim of our study is to investigate the comparative efficacy of high fidelity multi electrode ablation catheters vs the standard bipolar configuration in success of AV nodal ablation This study will provide insights on the use of new technology where application may increase efficacy, promote pat...

What is the current status of trial NCT03114124?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2017-05-23. Estimated completion is 2019-11-09.

What interventions are being tested in trial NCT03114124?

The interventions under investigation include: MIFI Catheter (DEVICE), Standard Ablation Catheter (DEVICE).

Who is sponsoring clinical trial NCT03114124?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03114124's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03114124, the US trial registry maintained by the National Library of Medicine. NCT03114124 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.