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The clinical study regarding effect of individualized PEEP on the occurrence of postoperative atelectasis in elderly patients undergoing laparoscopic colorectal surgery

The clinical study regarding effect of individualized PEEP on the occurrence of postoperative atelectasis in elderly patients undergoing laparoscopic colorectal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062869
Enrollment
Unknown
Registered
2022-08-22
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

postoperative pulmonary complications

Interventions

Group iPEEP (individual positive end-expiratory pressure):PEEP are titrated according to the optimal pulmonary static compliance (Cstat) method
Group fix PEEP:PEEP is set to a fixed 4 cmH2O

Sponsors

Beijing Friendship Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged 65-85 years; 2. Patients scheduled for laparoscopic colorectal surgery undergoing general anesthesia and surgical times are predicted to >= 2 hours; 3. BMI is 18-30 kg/m2; 4. American Society of Anesthesiologists(ASA) physical status I-III; 5. NYHA grades I-II; 6. Moderate or high risk for postoperative pulmonary complications.(Assess Respiratory Risk in Surgical Patients in Catalonia, ARISCAT>= 26).

Exclusion criteria

Exclusion criteria: 1. Patients with severe chronic obstructive pulmonary disease (COPD, GOLD grades III–IV), or a history of severe or uncontrolled bronchial asthma; 2. Patients with conditions that may affect the compliance of the respiratory system such as thoracic deformity, pneumothorax, and massive pleural effusion; 3. Patients with severe liver and kidney dysfunction; 4. Patients with a forced expiratory volume in the first second/forced vital capacity; (FEV1/FVC) ratio < 70%; 5. Patients with a smoking history within 8 weeks before surgery; 6. Patients expected to return to ICU after surgery; 7. Patients who refuse to participate in the experiment by themselves or their families.

Design outcomes

Primary

MeasureTime frame
Lung ultrasound score;

Secondary

MeasureTime frame
Incidence of Postoperative Pulmonary Complications;ventilation parameters;Anesthesia related parameters;30-day postoperative readmission rate;Quality of life assessment;Oxygenation Index;arterial blood gas;

Countries

China

Contacts

Public ContactXiaofang Hao

Beijing Friendship Hospital, Capital Medical University

ice-haoxiaofang@163.com+86 15201170075

Outcome results

None listed

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