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Impact of Negative Pressure Ventilation in Patients Hospitalized With Acute Hypercapnic Respiratory Failure

NCT06108284 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2026-02-13

No results posted yet for this study

Summary

The study aims to find if using a Biphasic Cuirass Ventilation is as effective as using a Non invasive Positive Pressure Ventilation in patients admitted with acute hypercapnic respiratory failure.

Conditions

  • Acute Hypercapnic Respiratory Failure

Interventions

DEVICE

Intervention Arm (Biphasic cuirass ventilation)

Patients in this arm will be placed on Biphasic cuirass ventilation

Sponsors & Collaborators

  • Hayek Medical

    collaborator UNKNOWN

  • University of Missouri-Columbia

    lead OTHER

Principal Investigators

  • Dennis Chairman, MD · University of Missouri-Columbia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-03
Primary Completion
2025-06-21
Completion
2025-06-21
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06108284 on ClinicalTrials.gov