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Clinical Evaluation of Physiological Closed-Loop Ventilation Modes

Clinical Evaluation of Physiological Closed-Loop Ventilation Modes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060586
Enrollment
Unknown
Registered
2022-06-05
Start date
2022-05-30
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Respiratory failure

Interventions

Test Group:Use Mindray Sv800 ventilator for ventilation
Control Group:Using G5 ventilator, SIMV mode

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients requiring invasive mechanical ventilation with an expected duration of mechanical ventilation of at least 48 hours; 2. Adult patients (>=18 years old) of any gender; 3. Patients who agree to participate in this trial and sign the "Informed Consent Form".

Exclusion criteria

Exclusion criteria: 1. Patients who are participating in other clinical trials; 2. Pregnant women; 3. Diseases leading to uncontrollable primary respiratory failure, such as patients with central respiratory failure, patients with respiratory failure due to neuromuscular disease (including High-level cervical spine injury), patients with end-stage cardiopulmonary failure, etc; 4. Patients with large lobe atelectasis, spontaneous pneumothorax, acute pulmonary embolism, cervical medullary injury and peripheral neuropathy; 5. Patients who are hemodynamically unstable and require high-dose vasoactive drugs; 6. Patients deemed unsuitable by the investigators.

Design outcomes

Primary

MeasureTime frame
Tidal volume;Blood oxygen saturation;End expiratory carbon dioxide partial pressure;

Secondary

MeasureTime frame
Heart rate;Mean arterial pressure;Minute ventilation;

Countries

China

Contacts

Public ContactGui Shuiqing

Shenzhen Second People's Hospital

18782198@qq.com+86 13713830562

Outcome results

None listed

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