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RECRUITING NA

NIV for Hypercapnic Respiratory Failure: AVAPS vs S/T BIPAP

NCT06047405 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this study is to compare two different modes of noninvasive ventilation in hypercapnic respiratory failure. The investigators will compare AVAPS and BIPAP S/T and hypothesize that AVAPS will result in a decreased length of stay in the ICU or on telemetry. Currently, noninvasive ventilation is the standard of care for hypercapnic respiratory failure. However, the most effective mode for patients with hypercapnic respiratory failure is unclear.

Interventions

  • DEVICE Average Volume-Assured Pressure Support (AVAPS)
  • DEVICE Bilevel Positive Airway Pressure Spontaneous Timed (BIPAP S/T)

Study Locations (1)

New York

  • Lenox Hill Hospital — New York

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2023-10-07
Est. Completion 2026-09-01
Phase NA

Sponsor

Northwell Health

371 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06047405

The ClinicalTrials.gov registry entry for NCT06047405 describes a study currently listed as recruiting. 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 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwell Health, which has 371 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 Hypercapnic Respiratory Failure appearing as the primary indexed condition, and to 2 interventions — of which Average Volume-Assured Pressure Support (AVAPS) 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: NCT06047405 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. 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 NCT06047405 about?

NCT06047405 is a clinical study titled "NIV for Hypercapnic Respiratory Failure: AVAPS vs S/T BIPAP". The goal of this study is to compare two different modes of noninvasive ventilation in hypercapnic respiratory failure. The investigators will compare AVAPS and BIPAP S/T and hypothesize that AVAPS will result in a decreased length of stay in the ICU or on telemetry. Currently, noninvasive ventilati...

What is the current status of trial NCT06047405?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2023-10-07. Estimated completion is 2026-09-01.

What conditions does trial NCT06047405 study?

This clinical trial studies the following conditions: Hypercapnic Respiratory Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06047405?

The interventions under investigation include: Average Volume-Assured Pressure Support (AVAPS) (DEVICE), Bilevel Positive Airway Pressure Spontaneous Timed (BIPAP S/T) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06047405?

This trial is sponsored by Northwell Health, which has 371 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06047405 being conducted?

This trial has 1 study location across New York. 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