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NCT03884660 · ClinicalTrials.gov registry record

remedē System Therapy Study

A clinical trial of Central Sleep Apnea, sponsored by Respicardia.

Active
Registry status
225
Enrollment target
20
Study locations

NCT03884660 is a study of Central Sleep Apnea that is active but no longer recruiting, run by Respicardia. The registered enrollment target is 225 participants, above the 94-participant average among 4 other Central Sleep Apnea trials with a reported enrollment target (139% higher). The trial reports 20 study locations across 14 states.

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The verdict

NCT03884660, a study of Central Sleep Apnea, is active but no longer recruiting, sponsored by Respicardia.

ACTIVE NOT RECRUITING
Registry status
225 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this non-randomized post market study is to collect clinical data on the safety and effectiveness of the remedē System in a real-world setting.

Conditions Studied

Interventions

  • DEVICE remede System

Study Locations (20)

Arizona

  • Banner University Medical Center - Phoenix
  • Arizona Heart Rhythm Center - Phoenix
  • HonorHealth - Scottsdale

North Carolina

  • Novant Health - Charlotte - Charlotte
  • East Carolina University - Greenville
  • Novant Health Forsyth Medical Center - Winston-Salem

Colorado

  • University of Colorado- Anschutz - Aurora
  • University of Colorado Health - Fort Collins

New York

  • Northwell Health - New Hyde Park
  • New York Presbyterian Hospital-Weill Cornell Medicine - New York

California

  • The University of California San Francisco - San Francisco

Florida

  • Central Florida Pulmonary Group - Orlando

Georgia

  • Emory University Midtown Hospital - Atlanta

Illinois

  • University of Chicago - Chicago

Trial Details

FieldValue
Enrollment Target 225 participants
Start Date 2019-06-18
Est. Completion 2030-12-30

Sponsor

Respicardia

8 total trials

What the Registry Record Tells You About NCT03884660

The ClinicalTrials.gov registry entry for NCT03884660 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 225 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 94-participant average among 4 other Central Sleep Apnea trials with a reported enrollment target (139% higher). The listed sponsor is Respicardia, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Central Sleep Apnea appearing as the primary indexed condition, and to 1 intervention - of which remede System is the first listed.

NCT03884660 reports 20 study locations spanning 14 distinct geographic areas - top geographies include Arizona, North Carolina, Colorado.

Frequently Asked Questions

What is clinical trial NCT03884660 about?

NCT03884660 is a clinical study titled "remedē System Therapy Study". The purpose of this non-randomized post market study is to collect clinical data on the safety and effectiveness of the remedē System in a real-world setting.

What is the current status of trial NCT03884660?

This trial is currently active not recruiting. The enrollment target is 225 participants. The study started on 2019-06-18. Estimated completion is 2030-12-30.

What conditions does trial NCT03884660 study?

This clinical trial studies the following conditions: Central Sleep Apnea.

What interventions are being tested in trial NCT03884660?

The interventions under investigation include: remede System (DEVICE).

Who is sponsoring clinical trial NCT03884660?

This trial is sponsored by Respicardia, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03884660 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Central Sleep Apnea

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.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.