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Timed Awake Prone and Repositioning for Patients With Covid-19-induced Hypoxic Respiratory Failure.

Efficacy of Timed Awake Prone and Repositioning in Patients With Covid-19-induced Hypoxic Respiratory Failure: a Multi-center, Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05689216
Enrollment
286
Registered
2023-01-19
Start date
2023-01-18
Completion date
2024-02-18
Last updated
2023-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corona Virus Infection, Hypoxic Respiratory Failure

Keywords

Awake prone positioning

Brief summary

Awake prone positioning has been reported to improve oxygenation for patients with COVID-19. Awake timed and repositioning is a novel method to improve patients' compliance and prolong the prone time. This study aims to explore the impact of timed prone and repositioning on the intubation rate and prognosis of COVID-19 patients with hypoxic respiratory failure.

Detailed description

Patients with COVID-19 may develop severe illness characterized by progressive hypoxic respiratory failure, resulting in the need for invasive mechanical ventilation. Reducing the rate of endotracheal intubation in patients with hypoxic respiratory failure can be beneficial to the prognosis, economize iatrical resources and reduce sanitary investment. Some studies have shown that prone positioning can improve oxygenation to some extent in patients receiving invasive mechanical ventilation due to severe ARDS. Whether awake prone positioning can reduce endotracheal intubation and mortality in COVID-19 patients with hypoxic respiratory failure is still controversial. A meta-analysis found that the awake prone positioning was safe and feasible to reduce the risk of intubation or death. However, the multicenter randomized controlled trial (RCT) conducted by Alhazzani et al pointed out that the awake prone positioning group did not significantly reduce the rate of endotracheal intubation when compared with the standard of care. Some researchers thought the time of prone positioning is an important factor for the different results. In previous studies, the median duration of prone positioning was only 4.8-5 hours per day but some guidelines recommend the duration should be more than 8 hours. Therefore, increasing patient adherence in the awake prone positioning and extending prone positioning time are of great importance. Awake timed prone and repositioning is a novel method proposed in recent years, which can improve patients' compliance and prolong the time of treatment. This study intends to ask whether awake timed prone and repositioning could impact the intubation rate and prognosis of unincubated patients with hypoxic respiratory failure induced by COVID-19.

Interventions

BEHAVIORALAwake timed prone and repositioning

Patients were instructed to adopt a timed prone and repositioning strategy with 4 sessions for four consecutive days. Session 1, lying on the belly; Session 2, lying on the right side; Session 3, sitting up; Session 4, lying on the left side; then back to session 1 (30 minutes to two hours for each session). The daily duration of timed prone and repositioning is strongly recommended for 8-10 hours.

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults ≥ 18 years of age * Awake patients without endotracheal intubation * Suspected or confirmed infection of COVID-19 * Hypoxemia requiring oxygen supplementation ≥ 0.4 FiO2 or ≥ 5L/min via nasal cannula * Bilateral or unilateral chest infiltrates on x-ray or HRCT * Admitted to the ICU or an acute care unit where hemodynamic and respiratory * Willingness to comply with the protocol and provide written informed consent

Exclusion criteria

* Risk of airway obstruction or even asphyxia * Need for emergent intubation after admission * Respiratory failure caused by cardiogenic pulmonary edema * Unable to implement timed prone and repositioning due to any cause * Injury or wound on the ventral body surface affecting the prone position * Unstable fracture of cervical vertebra and spine * Glaucoma or other sharp increases in intraocular pressure * Intracranial hypertension caused by traumatic brain injury etc. * Significantly high risk of pulmonary embolism * Acute hemorrhagic disease * Respiratory rate \>40 breaths/min, with significant dyspnea * Transcutaneous oxygen saturation can not be continuously monitored * Hemodynamic instability requiring vasoactive drugs (systolic blood pressure \<90 mmHg or mean arterial pressure \<65 mmHg despite adequate volume resuscitation) * Awareness disorder or inability to accept instructions, communication barrier with the nursing team, inability to use language or pager to call for help * Difficulty or limitation in autonomous movement, inability to adjust the position without assistance from others * Body mass index \> 37 kg/m2

Design outcomes

Primary

MeasureTime frameDescription
Endotracheal Intubation rateDay 30The incidence of endotracheal Intubation within 30 days of study enrollment

Secondary

MeasureTime frameDescription
Days of non-invasive ventilationDay 30Number of days alive and free of mechanical ventilation within 30 days of study enrollment
Days alive and outside the ICUDay 30Number of days alive and outside the ICU within 30 days of study enrollment
MortalityDay 30All-cause death within 30 days of study enrollment
Clinical eventsDay 30Clinical events include time to treatment failure( treatment failure defined as intubation or death); time to intubation; time to death; duration of invasive mechanical ventilation in intubated patients surviving to day 30; mortality in invasively mechanically ventilated patients; and physiological response to awake prone positioning, including the ratio of SpO2:FiO2 to respiratory rate, known as the ROX index.

Countries

China

Contacts

Primary ContactYuanyuan Yao, M.D.
yuanyuan58@126.com+86-18058783258

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026