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Evaluation of the effect of perioperative pre-warming techniques on preventing intraoperative hypothermia in elderly abdominal surgery: A randomized controlled trial

Evaluation of the effect of perioperative pre-warming techniques on preventing intraoperative hypothermia in elderly abdominal surgery: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126304
Enrollment
Unknown
Registered
2026-06-06
Start date
2026-06-10
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Perioperative Hypothermia

Interventions

Experimental group:Preoperative pre-warming: Before the patient is transferred from the ward to the operating room, an active forced-air warming blanket (product name: ZD Warming Blanket
model: WS100) manufactured by Zhende Medical Supplies Co., Ltd., is placed on the transfer stretcher. The device is turned on in advance, with the inflation temperature set to 42°C, and preheated for
Control group:Preoperative warming: Only routine cotton blankets are used for passive warming, without active forced-air pre-warming.

Sponsors

Xuanwu Hospital of Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients aged >= 60 years, of either sex; 2. Patients with an American Society of Anesthesiologists (ASA) physical status of I–III; 3. Undergoing elective abdominal surgery (including open abdominal surgery and laparoscopic abdominal surgery) under general anesthesia or combined general and neuraxial anesthesia; 4. Patients who voluntarily agree to participate in this study and sign the informed consent form (for patients unable to sign the informed consent form, the patient's legal guardian must sign the consent form on their behalf).

Exclusion criteria

Exclusion criteria: 1. Patients undergoing emergency surgery; 2. Patients with mental abnormalities or cognitive impairment; 3. Patients with hyperthyroidism or endocrine and metabolic disorders; 4. Patients who refuse to cooperate; 5. Pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Incidence of intraoperative hypothermia;

Secondary

MeasureTime frame
Anesthesia recovery time;Intraoperative blood loss;Incidence of postoperative delirium;Incidence of shivering;Patient thermal comfort score;

Countries

China

Contacts

Public ContactLiu Ting

Xuanwu Hospital of Capital Medical University

tingting9718@126.com+86 137 0128 9718

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026