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A Comparison of Rate Response Performance in Pacemaker Patients With an Indication of Sinus Node Dysfunction

NCT02027909 · View on ClinicalTrials.gov ↗

Study Summary

Providing ideal rate response to patients should improve their quality of life and ability to execute activities of daily living. Medtronic pacemakers provide rate response pacing by utilizing dual zone programming to specify an "activities of daily living" (ADL) response rate and an "exertion" response rate. There is much data to support the target heart rate for an exercise response but the data to support the programming of the ADL rate is lacking.

Conditions Studied

Interventions

  • DEVICE Reprogramming dual chamber pacemaker

Study Locations (1)

Tennessee

  • Wellmont CVA Heart Institute — Kingsport

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2011-11
Est. Completion 2015-04

Sponsor

Arun Rao

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02027909

The ClinicalTrials.gov registry entry for NCT02027909 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arun Rao, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Sinus Node Dysfunction appearing as the primary indexed condition, and to 1 intervention — of which Reprogramming dual chamber pacemaker is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02027909 reports 1 study location spanning 1 distinct geographic area — top geographies include Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02027909 about?

NCT02027909 is a clinical study titled "A Comparison of Rate Response Performance in Pacemaker Patients With an Indication of Sinus Node Dysfunction". Providing ideal rate response to patients should improve their quality of life and ability to execute activities of daily living. Medtronic pacemakers provide rate response pacing by utilizing dual zone programming to specify an "activities of daily living" (ADL) response rate and an "exertion" res...

What is the current status of trial NCT02027909?

This trial is currently completed. The enrollment target is 8 participants. The study started on 2011-11. Estimated completion is 2015-04.

What conditions does trial NCT02027909 study?

This clinical trial studies the following conditions: Sinus Node Dysfunction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02027909?

The interventions under investigation include: Reprogramming dual chamber pacemaker (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02027909?

This trial is sponsored by Arun Rao, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02027909 being conducted?

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

Related

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