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NCT07222410 · ClinicalTrials.gov registry record · NA

Closed Loop Oxygen Control in Chronic Obstructive Pulmonary Disease (COPD) Patients Treated With Nasal High Flow in the Hospital

A NA study of COPD, sponsored by Fisher and Paykel Healthcare.

Recruiting
Registry status
NA
Development phase
70
Enrollment target
1
Study location

NCT07222410 is a NA study of COPD that is actively recruiting participants, run by Fisher and Paykel Healthcare. The registered enrollment target is 70 participants, below the 2,418-participant average among 85 other COPD trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07222410, a NA study of COPD, is actively recruiting participants, sponsored by Fisher and Paykel Healthcare.

RECRUITING
Registry status
NA
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

The trial aims to evaluate whether the Airvo 3 device in OptiO2 mode can maintain patients' SpO2 levels within the target range better than manual oxygen titration in hospitalized COPD patients with hypoxemia/respiratory distress.

Conditions Studied

Interventions

  • DEVICE Closed loop oxygen control
  • DEVICE Manual titration

Study Locations (1)

New York

  • Icahn School of Medicine at Mount Sinai - New York

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2026-01-07
Est. Completion 2027-11
Phase NA

Sponsor

Fisher and Paykel Healthcare

25 total trials

What the Registry Record Tells You About NCT07222410

The ClinicalTrials.gov registry entry for NCT07222410 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,418-participant average among 85 other COPD trials with a reported enrollment target (97% lower). The listed sponsor is Fisher and Paykel Healthcare, which has 25 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with COPD appearing as the primary indexed condition, and to 2 interventions - of which Closed loop oxygen control is the first listed.

NCT07222410 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT07222410 about?

NCT07222410 is a clinical study titled "Closed Loop Oxygen Control in Chronic Obstructive Pulmonary Disease (COPD) Patients Treated With Nasal High Flow in the Hospital". The trial aims to evaluate whether the Airvo 3 device in OptiO2 mode can maintain patients' SpO2 levels within the target range better than manual oxygen titration in hospitalized COPD patients with hypoxemia/respiratory distress.

What is the current status of trial NCT07222410?

This trial is currently recruiting. It is a NA study. The enrollment target is 70 participants. The study started on 2026-01-07. Estimated completion is 2027-11.

What conditions does trial NCT07222410 study?

This clinical trial studies the following conditions: COPD.

What interventions are being tested in trial NCT07222410?

The interventions under investigation include: Closed loop oxygen control (DEVICE), Manual titration (DEVICE).

Who is sponsoring clinical trial NCT07222410?

This trial is sponsored by Fisher and Paykel Healthcare, which has 25 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07222410 being conducted?

This trial has 1 study location across New York. 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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