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Development of portable liquid insulation device and its effect on perioperative application in thoracoscopic radical resection of lung cancer

Development of portable liquid insulation device and its effect on perioperative application in thoracoscopic radical resection of lung cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072754
Enrollment
Unknown
Registered
2023-06-25
Start date
2021-03-10
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Lung cancer

Interventions

Conventional insulation group:All patients entered the operating room 30 minutes in advance and waited outside the room. After entering the room, intravenous puncture was performed, sodium Ringer acet
Experimental group:Conventional insulation+Disposable portable liquid insulation device

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
45 Years to 59 Years

Inclusion criteria

Inclusion criteria: ?45-59 years old male patients,ASA classification :I-II; (2) For patients undergoing radical operation of VATS for lung cancer under double-cavity tracheal intubation, static aspiration combined with general anesthesia, the operation duration was less than 3 hours; ? Body mass index (BMI) > 18.5kg/m2 < 25kg/m2; (4) Patients voluntarily participated in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: Subjects who meet any of the following criteria are excluded from this study. ? Preoperative external auditory canal disease, can not be measured tympanic membrane temperature; ? Preoperative temperature increases of over 37? or below 36?, intraoperative temperature increases of over 37?; ? Severe complications such as massive bleeding and shock occurred during the operation; ? hypothyroidism and hyperthyroidism; (5) autonomic nervous dysfunction; (6) Intraoperative transfusion; (7) Preoperative infection or suspected intraoperative infection of patients.

Design outcomes

Primary

MeasureTime frame
body temperature;

Secondary

MeasureTime frame
Chills;The time from patient transfer to PACU to extubation;

Countries

China

Contacts

Public ContactSun Zhaoxia

The First Affiliated Hospital of Guangzhou Medical Universityyi

870667534@qq.com+86 18122709185

Outcome results

None listed

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