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Comparative study of adaptive command ventilation and pressure support ventilation in patients undergoing mechanical ventilation, a single center randomized controlled trial

Comparative study of adaptive command ventilation and pressure support ventilation in patients undergoing mechanical ventilation, a single center randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076777
Enrollment
Unknown
Registered
2023-10-18
Start date
2023-10-20
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Mechanical ventilation patients

Interventions

Test group:First, collect respiratory mechanics indicators with pressure support ventilation for 30 minutes, and then use adaptive command ventilation for 30 minutes to collect respiratory mechanics i
control group:The indexes of respiratory mechanics were collected by adaptive command ventilation for 30 minutes, and then by pressure support ventilation for 30 minutes.

Sponsors

Yijishan Hospital of Wannan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Improvement or removal of the cause of mechanical ventilation; (2) Oxygenation index>200 mm Hg; Positive end expiratory pressure (PEEP) = 5-8 cm H2O; Inhalated oxygen concentration = 0.4; Arterial blood pH>7.30, arterial oxygen partial pressure>50 mm Hg; (3) Hemodynamics are stable and do not require treatment with vasoactive drugs or small doses of vasoactive drugs (such as dopamine<5-10 µ G · kg-1 · min-1); (4) Having the ability to breathe autonomously and effectively cough; (5) No blood sugar and electrolyte metabolism disorders; (6) No fever.

Exclusion criteria

Exclusion criteria: (1) Uncontrolled systemic infection; (2) Hemodynamic instability; (3) Previous or ongoing neuromuscular diseases such as myasthenia gravis and Guillain Jilin ballet syndrome

Design outcomes

Primary

MeasureTime frame
driving pressure;Work of Breathing;Peak pressure;

Secondary

MeasureTime frame
compliance;pplat;PEEPi;Oral closing pressure;The ratio of tidal volume to ideal body weight;PIP;Inspiratory peak flow rate;Inspiratory image resistance;Expiratory resistance;

Countries

China

Contacts

Public ContactYingying Wang

Yijishan Hospital of Wannan Meical Colleged

360972471@qq.com+86 183 7531 7778

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026