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A exploratory study of perioperative brain function on Tubeless VATS

A exploratory study of perioperative brain function on Tubeless VATS

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052463
Enrollment
Unknown
Registered
2021-10-27
Start date
2021-11-08
Completion date
Unknown
Last updated
2022-10-17

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:Video-assisted thoracoscopic surgery under tubeless anesthesia
Group 2:Video-assisted thoracoscopic surgery under intubation under general anesthesia

Sponsors

the First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Young and middle-aged group (18-59 years old): preoperative blood pressure and blood sugar are normal; no history of cerebral ischemia, cerebral infarction, no history of craniocerebral surgery and brain dysfunction, no history of mental and psychological disorders and medication; No history of gastrointestinal diseases, surgery, or immune-related diseases; no history of severe pain or continuous use of painkillers in the past 3 months; no history of alcoholism in the past 1 year; no malnutrition, no blindness or deafness; preoperative heart and lung function Normal, no history of allergy to anesthetics; wedge resection or lobectomy preparation for lung cancer admission; no contraindications for preoperative MRI, EEG and cerebral blood flow examination; 2. Elderly group (>=60 years old): preoperative blood pressure and blood sugar were normal, no obvious symptoms of cerebral infarction; no previous history of mental or psychological disorders or medication; no previous history of gastrointestinal diseases and surgery; preoperative heart and lung function No surgical contraindications; wedge resection or lobectomy preparation for lung cancer admission; no contraindications for preoperative MRI, EEG and cerebral blood flow examination; agreed to participate in the experimental group after communication.

Exclusion criteria

Exclusion criteria: 1. Obese patients with body mass index (BMI) >= 28kg/m2; 2. Anesthesia risk classification of American Society of Anesthesiology is above grade III; 3. Mallampati airway classification >= grade 3; 4. Gastrointestinal diseases have a high risk of reflux and gastrointestinal dysfunction; 5. Have a history of sleep apnea.

Design outcomes

Primary

MeasureTime frame
Brain Physiological Multimodal;

Secondary

MeasureTime frame
cerebral blood flow;Brain electrophysiology;cerebral oxygen metabolism;

Countries

China

Contacts

Public ContactHe Jianxing

the First Affiliated Hospital of Guangzhou Medical University

drjianxing.he@gmail.com+86 13802777270

Outcome results

None listed

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