Skip to content

Effects of permissive hypercapnia on cerebral oxygen supply and demand balance and recovery quality in elderly patients with cerebrovascular disease history undergoing thoracoscopic surgery

Effects of permissive hypercapnia on cerebral oxygen supply and demand balance and recovery quality in elderly patients with cerebrovascular disease history undergoing thoracoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064832
Enrollment
Unknown
Registered
2022-10-19
Start date
2022-10-19
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

None listed

Interventions

Group H:use protective lung ventilation strategies during surgery to maintain end-tidal carbon dioxide partial pressure at 50-65mmHg
Group L:do not use protective lung ventilation strategies during surgery to maintain end-tidal carbon dioxide partial pressure at 35-45mmHg

Sponsors

Department of Anesthesiology, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 65 years; 2. Plan for thoracoscopic lung surgery under general anesthesia; 3. Plan for intraoperative one-lung ventilation; 4. Previous cerebral infarction, luminal infarction, TIA, carotid artery stenosis or plaque that affects the blood supply to the brain; 5. Plan for anatomic lung resection; 6. Agree to participate and sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe lung dysfunction (including pneumonia, atelectasis, pleural effusion, acute lung injury, ARDS); 2. Severe renal insufficiency (preoperative renal replacement therapy); 3. Severe circulatory instability (severe coronary artery disease, unstable angina pectoris, left ventricular ejection fraction < 30%, sick sinus syndrome, severe sinus bradycardia <50 bpm, second degree or more severe atrioventricular block); 4. Diabetic patients; 5. Participate in other clinical trials within 30 days prior to randomization; 6. The responsible physician or endoscopist or anesthesiologist suggested other reasons for not participating in the experiment.

Design outcomes

Primary

MeasureTime frame
Cerebral desaturation (bilateral rSO2 reduction to 90% of baseline) event rate;

Secondary

MeasureTime frame
Cerebral oxygen saturation;Vasoactive drug use rate;Extubation time;Wake up time;Wake time;Incidence of agitation during recovery;PACU stay time;Incidence of nausea and vomiting 24 hours after operation;Incidence of delirium 24 hours after surgery;

Countries

China

Contacts

Public ContactWu Jingxiang

Department of Anesthesiology, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine

wjx1132@163.com+86 18930857186

Outcome results

None listed

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