Skip to content

Effects of individualized PEEP titration guided by driving pressure on pulmonary function and pulmonary complications in patients undergoing radical prostatectomy

Effects of driving pressure-directed individualized PEEP titration on postoperative pulmonary function and pulmonary complications in elderly patients with radical prostatectomy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058302
Enrollment
Unknown
Registered
2022-04-05
Start date
2022-04-06
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Prostate cancer

Interventions

Group P:individualized PEEP
Group C:traditional low level PEEP

Sponsors

The Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Pathological or cytological diagnosis of prostate cancer, laparoscopic radical resection of prostate cancer is proposed; 2. Aged >=65 years; BMI 18.5 ~ 25 kg/m^2; ASA grade ? or ?; 3. No obvious abnormality in lung function, no spinal cord or thoracic deformity, no difficult airway, asthma or COPD; 4. Estimated operation time >=2h; 5. Volunteers and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Preoperative hypertension was not controlled or poorly controlled (SBP>=180mmHg or DBP>=110mmHg); 2. Severe respiratory complications (including but not limited to COPD, bullae, bronchiectasis, asthma, severe sleep apnea syndrome, pulmonary interstitial fibrosis, pulmonary heart disease, recent respiratory failure, etc.); 3. Severe damage of liver and kidney function; Severe cardiovascular diseases: such as severe coronary atherosclerosis, heart failure, myocardial infarction and other underlying diseases; 4. Participated in other clinical studies within the last 3 months; 5. Situations that other researchers consider inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Perioperative lung function;Postoperative pulmonary complications;

Secondary

MeasureTime frame
Intraoperative respiratory mechanics;

Countries

China

Contacts

Public ContactLi Yun
yunli_001@aliyun.com+86 15105517565

Outcome results

None listed

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