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Study on lung protective ventilation strategy for patients undergoing major craniotomy

Study on lung protective ventilation strategy for patients undergoing major craniotomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013048
Enrollment
Unknown
Registered
2017-10-19
Start date
2017-10-19
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

major craniotomy

Interventions

experimental group 1:Traditional strategy of lung protective ventilation
experimental group 2:Lung protective ventilation strategy under optimal peep

Sponsors

The Second Affiliated Hospital of Medical College of Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients and their families signed informed consent; ASA 1-3 grade; over 18 years of age; brain tumors, cerebral aneurysm, cerebral vascular malformation; the operation time more than 3 hours; a BMI of 18 ~ 25kg/m2.

Exclusion criteria

Exclusion criteria: Preoperative radiotherapy in patients with heart failure; ALI/ARDS; or suspected with heart failure; 15 days before operation and received mechanical ventilation (CPAP) treatment; pneumothorax or lung bullae; severe liver and kidney dysfunction; COPD patients who need oxygen therapy or CPAP; postoperative into ICU or postoperative consciousness did not recover; is participating in other clinical intervention trials.

Design outcomes

Primary

MeasureTime frame
Postoperative pulmonary complications;

Secondary

MeasureTime frame
Improved lung infection score;Inflammation factor detection;

Countries

China

Contacts

Public ContactLina Yu

The Second Affiliated Hospital of Medical College of Zhejiang University

chinalian2@163.com+86 13958033387

Outcome results

None listed

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