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NCT01061125 · ClinicalTrials.gov registry record

Implantable Loop Recorders in Post-atrial Fibrillation (AF) Ablation: RPAF-A

A clinical trial of Atrial Fibrillation, sponsored by The Cleveland Clinic.

Completed
Registry status
68
Enrollment target
1
Study location

NCT01061125 is a study of Atrial Fibrillation that has completed, run by The Cleveland Clinic. The registered enrollment target is 68 participants, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01061125, a study of Atrial Fibrillation, has completed, sponsored by The Cleveland Clinic.

COMPLETED
Registry status
68 participants
Enrollment target
1
Study location

Study Summary

This is a randomized pilot study, of post pulmonary vein isolation (PVI) patients to determine the clinical utility of the Implantable Loop Recorder. These type of patients either are monitored with weekly transtelephonic monitoring (TTM) or implantable loop recorder (ILR). The Medtronic Reveal XT loop recorder will be implanted at the time of the PVI or at the 3-4 month PVI follow-up visit and patient care will be managed based on randomization to a blinded or unblinded group. Outcome measures will be compared to aid in decision making regarding anticoagulation and overall post ablation clinical management.

Conditions Studied

Interventions

  • OTHER TTM and Holter monitor

Study Locations (1)

Ohio

  • Cleveland Clinic - Cleveland

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2010-01
Est. Completion 2016-10

Sponsor

The Cleveland Clinic

688 total trials

What the Registry Record Tells You About NCT01061125

The ClinicalTrials.gov registry entry for NCT01061125 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 68 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,997-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (98% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention - of which TTM and Holter monitor is the first listed.

NCT01061125 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT01061125 about?

NCT01061125 is a clinical study titled "Implantable Loop Recorders in Post-atrial Fibrillation (AF) Ablation: RPAF-A". This is a randomized pilot study, of post pulmonary vein isolation (PVI) patients to determine the clinical utility of the Implantable Loop Recorder. These type of patients either are monitored with weekly transtelephonic monitoring (TTM) or implantable loop recorder (ILR). The Medtronic Reveal XT l...

What is the current status of trial NCT01061125?

This trial is currently completed. The enrollment target is 68 participants. The study started on 2010-01. Estimated completion is 2016-10.

What conditions does trial NCT01061125 study?

This clinical trial studies the following conditions: Atrial Fibrillation.

What interventions are being tested in trial NCT01061125?

The interventions under investigation include: TTM and Holter monitor (OTHER).

Who is sponsoring clinical trial NCT01061125?

This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01061125 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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