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

NCT01537237 · ClinicalTrials.gov registry record

Comparison of Rotational Angiography/Electroanatomical Mapping Fusion Versus CT/Electroanatomical Mapping Fusion to Guide AF Ablation

A clinical trial of Atrial Fibrillation and Arrhythmia, sponsored by Steward St. Elizabeth's Medical Center of Boston.

Completed
Registry status
37
Enrollment target
2
Study locations

NCT01537237: Completed study of Atrial Fibrillation and Arrhythmia, sponsored by Steward St. Elizabeth's Medical Center of Boston.

NCT01537237 is a study of Atrial Fibrillation and Arrhythmia that has completed, run by Steward St. Elizabeth's Medical Center of Boston. The registered enrollment target is 37 participants, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (99% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01537237, a study of Atrial Fibrillation and Arrhythmia, has completed, sponsored by Steward St. Elizabeth's Medical Center of Boston.

COMPLETED
Registry status
37 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to compare rotational angiography (3DATG technology)intra-procedure (during the ablation procedure) with CT (x-ray) pre-procedure (before the ablation procedure) fusion to create an anatomical picture of a heart to help adequately guide an ablation procedure for patients with arrhythmias.

Primary Outcome

Case report forms were created to capture intraprocedure data (i.e.noticeable map drift) of the maps created and used to create ablation lesions. Procedure user's overall clinical evaluation (i.e.feedback) and experience (i.e. radiation time, number of mapping points collected per map, mapping time) will also be collected and analyzed. And patients will be followed as routine for overall disease evaluation (i.e. ECG and patient reported symptoms) within 6 months from the procedure.

Study Locations (2)

Florida

  • Holy Cross Hospital - Fort Lauderdale

Massachusetts

  • St. Elizabeth's Medical Center - Brighton

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2011-08
Est. Completion 2014-11

What the finished NCT01537237 record still lists

NCT01537237 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 37 participants, a relatively small participant target, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (99% lower).

The record links to 2 conditions, with Atrial Fibrillation appearing as the primary indexed condition, and to 0 interventions.

NCT01537237 reports a single indexed study location in Florida, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT01537237 about?

NCT01537237 is a clinical study titled "Comparison of Rotational Angiography/Electroanatomical Mapping Fusion Versus CT/Electroanatomical Mapping Fusion to Guide AF Ablation". The purpose of this study is to compare rotational angiography (3DATG technology)intra-procedure (during the ablation procedure) with CT (x-ray) pre-procedure (before the ablation procedure) fusion to create an anatomical picture of a heart to help adequately guide an ablation procedure for patients...

What is the current status of trial NCT01537237?

This trial is currently completed. The enrollment target is 37 participants. The study started on 2011-08. Estimated completion is 2014-11.

What conditions does trial NCT01537237 study?

This clinical trial studies the following conditions: Atrial Fibrillation, Arrhythmia.

Who is sponsoring clinical trial NCT01537237?

This trial is sponsored by Steward St. Elizabeth's Medical Center of Boston, which has 18 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01537237 being conducted?

This trial has 2 study locations across Florida, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Atrial Fibrillation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01537237's enrollment target sits among peer trials

37 184th of 202 higher than 19 of 202 other Atrial Fibrillation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Atrial Fibrillation 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

  • NCT02800486 · 37 participants · Phase 2

    Super Selective Intra-arterial Repeated Infusion of Cetuximab (Erbitux) With Reirradiation for Treatment of Relapsed/Refractory GBM, AA, and AOA

  • NCT03173937 · 37 participants · Phase 1

    Unrelated Umbilical Cord Blood Transplantation for Severe Aplastic Anemia and Hypo-plastic MDS Using CordIn(TM), Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells to Expedite Engraftment and Improve Transplant Outcome

  • NCT03295227 · 37 participants · Phase 1

    Pembrolizumab in Treating Participants With Unresectable Thymoma or Thymic Cancer

  • NCT03401047 · 37 participants · Early Phase 1

    Study to Assess Potential Impairments in Estradiol Augmentation of Gonadotropin Secretion in Polycystic Ovary Syndrome

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01537237, the US trial registry maintained by the National Library of Medicine. NCT01537237 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.