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Effects of tidal volume on mechanical power under individualized PEEP: A prospective, single-center, randomized crossover study

Effects of tidal volume on mechanical power under individualized PEEP: A prospective, single-center, randomized crossover study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097259
Enrollment
Unknown
Registered
2025-02-17
Start date
2025-02-17
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

None

Interventions

VT6:Each patient underwent mechanical ventilation at 3 tidal volume levels in random order, and the respiratory mechanical indexes of each tidal volume level were measured 5 minutes after the respirat
VT8:Each patient underwent mechanical ventilation at 3 tidal volume levels in random order, and the respiratory mechanical indexes of each tidal volume level were measured 5 minutes after the respirat
VT10:Each patient underwent mechanical ventilation at 3 tidal volume levels in random order, and the respiratory mechanical indexes of each tidal volume level were measured 5 minutes after the respira

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age over 18 years old; 2.ASA class I-III; 3.BMI between 18kg/m2 and 30kg/m2; 4.Scheduled for abdominal surgery; 5.Informed and willing to participate in the trial, and willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.History of severe lung diseases, such as chronic obstructive pulmonary disease, severe asthma, thoracic and spinal malformations, pleural effusion, pneumothorax and giant bulla, pulmonary surgery and other diseases affecting respiratory compliance 2.Severe cardiac, hepatic, renal, or hematologic disorders; 3.Central nervous system disorders impairing respiratory function; 4.Contraindications for PEEP use: intracranial hypertension, bronchopleural fistula, hypovolemic shock, etc.; 5.Participation in other clinical studies within the last 3 months; 6.Patients who refuse to participate in the trial or cannot cooperate.

Design outcomes

Primary

MeasureTime frame
Mechanical power;

Secondary

MeasureTime frame
Mechanical ventilation parameter;Arterial blood gas;Postoperative pulmonary complications;

Countries

China

Contacts

Public ContactLijian Chen

The First Affiliated Hospital of Anhui Medical University

chenlijian77@126.com+86 139 6669 9467

Outcome results

None listed

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