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Comparison of forced-air-warming blanket and intravenous fluid warming device on the prevention of intraoperative hypothermia in patients undergoing general surgery

Comparison of forced-air-warming blanket and intravenous fluid warming device on the prevention of intraoperative hypothermia in patients undergoing general surgery: A prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033142
Enrollment
Unknown
Registered
2020-05-22
Start date
2018-10-07
Completion date
Unknown
Last updated
2020-05-25

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

Conditions

General surgical disease

Interventions

Group 1:using blanket to cover patient
Group 2:using blanket and FAW to cover patient
Group 3:using blanket to cover patient and using warmed iv fluid
Group 4:using blanket and FAW to cover patientand using warmed iv fluid

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. General anesthesia, ASA class I, II; 2. Open surgery of general surgery and supine position; 3. Aged 18 to 65 years old, basic communication skills; 4. Operation time >=1 hour.

Exclusion criteria

Exclusion criteria: 1. Abnormal preoperative body temperature; 2. Patients with thermoregulatory disorders or basic metabolic diseases (such as hyperthyroidism and obesity); 3. Infection or abnormal body temperature existed in the preoperative 3d; 4. Preoperative use of corticosteroid or immunosuppressive agents; 5. Pregnant women.

Design outcomes

Primary

MeasureTime frame
Hypothermia incidence;coagulation function;Postoperative extubation duration;

Secondary

MeasureTime frame
The incidence of SSI;Incidence of chills;Postoperative PACU resuscitation time;

Countries

China

Contacts

Public ContactAnque Liao

West China Hospital, Sichuan University

1017485960@qq.com+86 13558626845

Outcome results

None listed

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