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

COMPLETED NA

Janus Feasibility Study

NCT03985527 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this feasibility study is to assess whether an alternative transvenous lead location affects respiration and airway physiology during a commercial remedē® System or commercial transvenous cardiac device (de novo pacemaker or implantable cardiac defibrillator) implant procedure.

Conditions Studied

Interventions

  • DEVICE Transvenous nerve stimulation

Study Locations (3)

North Carolina

  • Novant Health Forsyth Medical Center — Winston-Salem

Ohio

  • The Ohio State University Wexner Medical Center — Columbus

Pennsylvania

  • Bryn Mawr Medical Specialists Association — Bryn Mawr

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2020-01-09
Est. Completion 2025-12-12
Phase NA

Sponsor

Respicardia

3 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03985527

The ClinicalTrials.gov registry entry for NCT03985527 describes a study currently listed as completed. It is categorized as NA, 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 29 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Respicardia, which has 3 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 Sleep Apnea Syndromes appearing as the primary indexed condition, and to 1 intervention — of which Transvenous nerve stimulation 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: NCT03985527 reports 3 study locations spanning 3 distinct geographic areas — top geographies include North Carolina, Ohio, Pennsylvania. 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 NCT03985527 about?

NCT03985527 is a clinical study titled "Janus Feasibility Study". The purpose of this feasibility study is to assess whether an alternative transvenous lead location affects respiration and airway physiology during a commercial remedē® System or commercial transvenous cardiac device (de novo pacemaker or implantable cardiac defibrillator) implant procedure.

What is the current status of trial NCT03985527?

This trial is currently completed. It is a NA study. The enrollment target is 29 participants. The study started on 2020-01-09. Estimated completion is 2025-12-12.

What conditions does trial NCT03985527 study?

This clinical trial studies the following conditions: Sleep Apnea Syndromes. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03985527?

The interventions under investigation include: Transvenous nerve stimulation (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03985527?

This trial is sponsored by Respicardia, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03985527 being conducted?

This trial has 3 study locations across North Carolina, Ohio, Pennsylvania. 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