Skip to content

A prospective, randomized controlled clinical trial of the effects of different anesthesia methods on postoperative immune function in patients with lung cancer

A prospective, randomized controlled clinical trial of the effects of different anesthesia methods on postoperative immune function in patients with lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038530
Enrollment
Unknown
Registered
2020-09-23
Start date
2020-09-18
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Lung cancer

Interventions

Group 1:Total intravenous anesthesia
Group 2:Intravenous-inhalation compound general anesthesia

Sponsors

Cancer Hospital Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 40 patients with stage I and stage II lung cancer who are planning to undergo thoracoscopic surgery, aged 18-70 years, ASA I-III grade.

Exclusion criteria

Exclusion criteria: (1) preoperative anemia: male Hb 37.5 degree C the day before surgery; (3) lungs before surgery Ventilation dysfunction; (4) Pulmonary infection, bronchial asthma or airway hyperresponsiveness before surgery; (5) Past thoracic surgery history; (6) Cardiac function above grade II; (7) Patients with hypertension, Preoperative systolic blood pressure> 140 mmHg and/or diastolic blood pressure> 90 mmHg; (8) Preoperative congenital heart disease, valvular disease, coronary heart disease, arrhythmia; (9) Central nervous system disease, history of stroke; (10) Combined with liver dysfunction and renal dysfunction; (11) history of preoperative radiotherapy and chemotherapy; (12) Postoperative diagnosis of stage III and IV lung cancer patients.

Design outcomes

Primary

MeasureTime frame
VEGF-c, TGF-beta, IL-6, IL-10, IFN-gama, TNF-alpha;

Secondary

MeasureTime frame
VRS at 24h and 48h after surgery;

Countries

China

Contacts

Public ContactGuo Zhixing

Department of Anesthesiology, Cancer Hospital, Chinese Academy of Medical Sciences

xingbj2000@126.com+86 13811348296

Outcome results

None listed

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