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Application of an intelligent closed-loop thermal insulation system for intraoperative thermoprotection in patients undergoing gynaecological malignancy surgery: a single-centre randomised controlled clinical trial

Application of an intelligent closed-loop thermal insulation system for intraoperative thermoprotection in patients undergoing gynaecological malignancy surgery: a single-centre randomised controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119233
Enrollment
Unknown
Registered
2026-02-24
Start date
2025-03-26
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Hypothermia

Interventions

Intelligent heating blanket set:After the patient was transferred to the operating table, the closed-loop insulation mode was activated, and the target heating system was used for insulation. The expe
Ordinary heating blanket set:When the patients body temperature is below 36?, set the temperature of the thermal blanket to 39?. When the patients body temperature is between 36? and 37?, set the temp

Sponsors

Henan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age > 18 years old; 2.ASA Grade I -III; 3.The operation lasts for more than 3 hours; 4.Subjects with gynecological malignant tumors who are undergoing elective general anesthesia and laparotomy; 5.Be able to understand the process and methods of this research, voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Those with contraindications to general anesthesia or a history of anesthesia accidents in the past; 2.Uncontrolled diabetes or hypertension; 3.History of alcohol abuse or drug dependence; 4.morbidly obese individuals; 5.Those with a history of mental illness; 6.Has a severe history of skin allergies, especially to silicone or medical plastics; 7.Patients who want to withdraw halfway through the experiment. 8. Participants who, in the opinion of the researcher, have any other factors that make them unsuitable for this trial.

Design outcomes

Primary

MeasureTime frame
The incidence of intraoperative hypothermia in patients;

Countries

China

Contacts

Public ContactJiaqiang Zhang

Henan Provincial People's Hospital

2306287704@qq.com+86 139 3712 1360

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026