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Staying Warm for a Better Recovery: The Impact of Perioperative Warming in Thoracic Surgery

Staying Warm for a Better Recovery: The Impact of Perioperative Warming in Thoracic Surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117493
Enrollment
Unknown
Registered
2026-01-26
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Thoracic Surgery Diseases

Interventions

Group A :Group A received conventional perioperative nursing care without specialized warming measures
Group B:Group B was administered standard cotton blanket warming as the basic thermal management approach
Group C:Group C underwent an evidence-based perioperative warming protocol incorporating multiple validated temperature maintenance strategies throughout the surgical pathway

Sponsors

Zhuhai Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. complete clinical data; 2. 18 years <= age < 90 years; 3. with indications for surgery: with normal cardiac, hepatic and renal function; 4. No contraindications to surgery and no contraindications to anaesthesia; 5. American Society of Anaesthesiologists ASA classification I to III; 6. Body mass index (BMI): 18.6 to 29.7 kg/m^2; 7. patients were all conscious and had stable vital signs.

Exclusion criteria

Exclusion criteria: 1. Presence of coagulation disorders; 2. Presence of anaesthetic allergy; 3. patients with severe hepatic or renal insufficiency; 4. patients with infectious diseases; 5. Patients with severe cardiovascular and cerebrovascular diseases; 6. patients with long-term abuse of sedative drugs, opioids, drugs affecting cognitive function and delirium; 7. patients with a previous history of chest surgery; 8. Oral temperature 37.5°C at the time of admission; 9. Those who are unable to cooperate with the study due to severe audio-visual disorders, psychological disorders and or mental disorders; 10. Accidental resuscitation during the operation, admission to ICU for postoperative supervision, and the test could not be continued to be completed; 11. Loss of postoperative visits or inability to co-operate with the study for any reason.

Design outcomes

Primary

MeasureTime frame
core body temperature;Perioperative related indicators;Loop function;Complication rate;Immune function indicators;

Countries

China

Contacts

Public ContactLiu Juan

Zhuhai Hospital of Southern Medical University

493102678@qq.com+86 159 7530 8264

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026