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Using wireless thermometer monitoring to investigate whether preoperative warming can enhance postoperative recovery in colorectal cancer surgery patients

Efficacy of Perioperative Warming with Wireless Temperature Monitoring in Laparoscopic Colorectal Cancer Resection: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124213
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Colorectal tumors requiring elective radical resection

Interventions

Routine temperature management group:Preoperative light blanket coverage
Pre-warming group:Preoperative pre-warming

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 75 years, of any gender; 2. Patients scheduled for elective laparoscopic radical resection of colorectal cancer under general anesthesia; 3. Signed informed consent obtained; 4. Preoperative body temperature within the normal range; 5. American Society of Anesthesiologists (ASA) physical status classification I to III; 6. Body mass index (BMI) between 18.5 and 28 kg/m²; 7. Surgical duration between 2 and 6 hours.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of severe skin allergies, particularly to silicone or medical-grade plastic; 2. Patients requiring intravenous access in both upper limbs (as the wireless temperature sensor needs to be placed in the axilla without an IV line to avoid interference with temperature monitoring accuracy due to cold fluids); 3. Patients with preoperative visual, hearing, or verbal communication impairments; 4. Patients with severe immune system abnormalities (such as hyperthyroidism, hypothyroidism, or adrenocortical insufficiency) or sweat gland dysfunction; 5. Patients with coagulation disorders, cachexia, or burn injuries; 6. Conversion from laparoscopic surgery to open surgery.

Design outcomes

Primary

MeasureTime frame
Perioperative hypothermia incidence;

Secondary

MeasureTime frame
Time to Hypothermia after Induction;Postoperative hospital stay;Patient satisfaction;Postoperative complications;Duration of Hypothermia;Quality of emergence;Complications associated with hypothermia;Presence of fever;Physician Satisfaction;total cost during the period from surgery to discharge;Nurse Satisfaction;Effect of fever management;

Countries

China

Contacts

Public ContactDai Qinxue

The First Affiliated Hospital of Wenzhou Medical University

653091408@qq.com+86 13695842272

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026