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NCT06089694 · ClinicalTrials.gov registry record

Crome/Cobalt Respiration Study

A clinical trial, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

Completed
Registry status
61
Enrollment target

NCT06089694: Completed study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

NCT06089694 is a clinical trial that has completed, run by Medtronic Cardiac Rhythm and Heart Failure. The registered enrollment target is 61 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06089694 has completed, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

COMPLETED
Registry status
61 participants
Enrollment target

Study Summary

The goal of this study is to compare measured respiration rates in various subject scenarios and use conditions between capnography and the Crome and Cobalt ICD and CRT-D MRI SureScan devices (derived using a Holter recorder).

Primary Outcome

Daily respiration rates will be calculated using a series of paired device-derived respiration rates and capnography waveform-derived respiration rates, where the capnography respiration rate will be the source of truth. The differences in these daily respiration rates will be evaluated to determine whether the daily device-derived respiration rate accuracy is acceptable (i.e., consistently within +/- 3 breaths per minute of the true respiration rate).

Interventions

  • DEVICE Enabling Sensor Research Holter Mode feature

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2023-11-21
Est. Completion 2024-06-12

What the finished NCT06089694 record still lists

NCT06089694 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 61 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Enabling Sensor Research Holter Mode feature is the first listed.

NCT06089694 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06089694 about?

NCT06089694 is a clinical study titled "Crome/Cobalt Respiration Study". The goal of this study is to compare measured respiration rates in various subject scenarios and use conditions between capnography and the Crome and Cobalt ICD and CRT-D MRI SureScan devices (derived using a Holter recorder).

What is the current status of trial NCT06089694?

This trial is currently completed. The enrollment target is 61 participants. The study started on 2023-11-21. Estimated completion is 2024-06-12.

What interventions are being tested in trial NCT06089694?

The interventions under investigation include: Enabling Sensor Research Holter Mode feature (DEVICE).

Who is sponsoring clinical trial NCT06089694?

This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, which has 115 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT06089694, the US trial registry maintained by the National Library of Medicine. NCT06089694 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.