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HYPoxaEmic Respiratory Failure and Awake Prone Ventilation

NCT05990101 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 262

Last updated 2023-08-14

No results posted yet for this study

Summary

The goal of this prospective multi-centre randomised controlled trial is to determine if addition of awake prone positioning to standard oxygen, high flow oxygen therapy and non-invasive ventilation may reduce the rates of endotracheal intubation and mechanical ventilation.

Conditions

Interventions

BEHAVIORAL

Awake prone position (APP)

Awake prone position for 4 or more hours per day for the first 72 hours following randomisation.

Sponsors & Collaborators

  • Vilnius University Hospital Santaros Klinikos

    collaborator OTHER

  • Vilnius University

    lead OTHER

Principal Investigators

  • Ieva Jovaisiene, Dr · Vilnius University Hospital Santaros Klinikos

  • Mandeep K Phull, Dr · Barking, Havering and Redbridge University Hospitals NHS Trust

  • Tomas Jovaisa, Prof · Vilnius University Hospital Santaros Klinikos

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-12
Primary Completion
2026-08-01
Completion
2028-09-01

Countries

  • Lithuania
  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

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 NCT05990101 on ClinicalTrials.gov