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Effect of PP in Patients With Ultra-low VT

S

Southeast University, China

Status

Enrolling

Conditions

Tidal Volume
Prone Position
Acute Respiratory Distress Syndrome

Treatments

Other: position

Study type

Observational

Funder types

Other

Identifiers

NCT06215209
Ultra-low VT and PP

Details and patient eligibility

About

Acute respiratory distress syndrome (ARDS) is a heterogeneous syndrome with similar clinicopathological feathers caused by different etiologies. Respiratory supportive strategies is the main ARDS management, and the guidelines recommend low tidal volume to improve clinical outcomes. To be note, overdistension can still occur even if using a tidal volume as low as 6 ml/kg, given the heterogeneous nature of the syndrome. Therefore, adjusting tidal volume level to less than 6ml/kg may reduce ventilator-induced lung injury (VILI) and thus improve outcomes, especially in patients with severe lung injury. Prone position is also an important management in severe ARDS. Prone position can improve ventilation-perfusion (V/Q) matching and reduce the risk of VILI by recruiting dorsal collapsed alveoli. Meanwhile, prone position has also been shown to improve hemodynamics. Recent studies have showed that prone position did not reduce duration of venovenous extracorporeal membrane oxygenation (VV-ECMO) and 90-day mortality in patients with ARDS who receive VV-ECMO with ultra-low tidal volume ventilation. Therefore, the effect of PP on ventilation and lung blood flow in ARDS patients treated with VV-ECMO wiht ultra-low tidal volume ventilation remains unclear.

Enrollment

45 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients were enrolled if they were undergoing invasive mechanical ventilation and were supported by VV-ECMO for less than 48 hours

Exclusion criteria

  • younger than 18 years old
  • contraindications for prone position ventilation
  • past chronic respiratory diseases (long-term family oxygen therapy for chronic
  • respiratory diseases such as pulmonary fibrosis or COPD)
  • New York Heart Association class above II
  • contraindications to the use of EIT (e.g., presence of pacemaker or chest surgical wounds dressing) or prone position (as decided by the attending physician)
  • severe hemodynamic instability
  • gave written or witnessed verbal informed consent

Trial design

45 participants in 1 patient group

ultra-low tidal volume group
Description:
ARDS patients with ultra-low tidal volume ventilation
Treatment:
Other: position

Trial contacts and locations

1

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Central trial contact

liu ling, phD

Data sourced from clinicaltrials.gov

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