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A randomized controlled multicenter study of warming for patients in endoscopic surgery with Intraoperative flushing

A randomized controlled multicenter study of warming for patients in endoscopic surgery with Intraoperative flushing

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084999
Enrollment
Unknown
Registered
2024-05-29
Start date
2024-06-01
Completion date
Unknown
Last updated
2026-06-15

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:Intervention A: Disposable thermal blankets were used for inflatable heating before and during surgery. Intervention B: Disposable thermal blankets were used for inflatable heating
Blank control group:control groups,No insulation

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provincial People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) =18 years old, male or female (2)Elective general anesthesia, intralesional anesthesia, or nerve block anesthesia for surgery; including electrocutaneous prostatectomy, transureteroscopy, cystoscopy, percutaneous nephrolithotomy for renal calculi, shoulder arthroscopy, and knee arthroscopy (3) Surgical time: =30min, =150min (4) Preoperative temperature <37.3°C (5) Normal preoperative coagulation time

Exclusion criteria

Exclusion criteria: (1) Mental illness (2) Patients with hyper/hypometabolic disorders with high or low basal hypothermia (patients with central hyperthermia including central hyperthermia due to cerebrovascular disease, traumatic brain injury and surgery, epilepsy, and acute hydrocephalus; and thermoregulatory abnormalities including Malignant Hyperthermia (MHS), Neuroleptic Malignant Syndrome, and patients with a clear diagnosis of hypothyroidism or hyperthyroidism who have a current abnormal metabolic profile); (3) Damage to the skin's insulation barrier such as extensive skin burns (4) Infectious fever (5) Other causes of body temperature higher than 38.5 ? three days before surgery; (6) Other persons who, in the opinion of the investigator, are not suitable for participation in the clinical trial;

Design outcomes

Primary

MeasureTime frame
body temperature;room temperature;Volume of rinsing liquid;Duration of surgery;Duration of anesthesia;Duration of insulation;

Secondary

MeasureTime frame
adverse event;Duration of hospitalization;hospitalization cost;

Countries

China

Contacts

Public ContactLie Qian

Sichuan Academy of Medical Sciences & Sichuan Provincial People’s Hospital

leiqianggh@163.com+86 150 1318 9601

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026