Hypothermia; Anesthesia Clinical Trial
Official title:
Establishment of Systemic Prevention and Management for Perioperative Hypothermia and Its Effect on Patients Outcome—a Prospective Multiple Centers Randomized Controlled Study
This is a randomized, single-blinded, multi-center study clinical trial to determine both clinical and health outcomes of stratified warm strategy to prevent intraoperative hypothermia. Participants enrolled into this trial will be from elective major surgery population in PUMC Hospital, Beijing Hospital and Xuanwu Hospital. investigators plan to enroll approximately 800 participants. Hypothermia risk will be evaluated through PREDICTOR model in all participants. According to hypothermia risk level, these participants will be stratefied into high, moderate and low risk group. Participants in each group will be randomly categorize into warm group and control group. Active warm and fluid warm strategy, prewarm and fluid warm strategy and only prewarm strategy are used for high risk, moderate risk and low risk patients seperately. For controll group traditional passive warm was used.
Status | Not yet recruiting |
Enrollment | 800 |
Est. completion date | August 31, 2021 |
Est. primary completion date | March 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Age=18 Core temperature preoperation =36.0 ? and =37.5? ASA I-III Informed consent Exclusion Criteria: - emergency operation - uncontrolled diebete mellitus with insulin treatment (preoperative blood glucose>250mg/dL) - hyperthyroidism and hypothyroidism - Raynaud's disease - patients with hematopathy and immune disease - anticoagulant and non-steroid anti-inflammatory drug intake with 14 days before operation - infectious fever within 4 weeks before operation - laboratory abnomality as follow - Hemoglobin=10.0g/L - Platelet=100,000/ml - White blood cell<3000/dl or>14,000/dl - Fibrinogen<200mg/dL - Thrombin time>40 second - International normalized ratio<70% |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Peking Union Medical College Hospital | Beijing Hospital, Xuanwu Hospital, Beijing |
Yi J, Lei Y, Xu S, Si Y, Li S, Xia Z, Shi Y, Gu X, Yu J, Xu G, Gu E, Yu Y, Chen Y, Jia H, Wang Y, Wang X, Chai X, Jin X, Chen J, Xu M, Xiong J, Wang G, Lu K, Yu W, Lei W, Qin Z, Xiang J, Li L, Xiang Z, Pan S, Zhan L, Qiu K, Yao M, Huang Y. Intraoperative — View Citation
Yi J, Xiang Z, Deng X, Fan T, Fu R, Geng W, Guo R, He N, Li C, Li L, Li M, Li T, Tian M, Wang G, Wang L, Wang T, Wu A, Wu D, Xue X, Xu M, Yang X, Yang Z, Yuan J, Zhao Q, Zhou G, Zuo M, Pan S, Zhan L, Yao M, Huang Y. Incidence of Inadvertent Intraoperative Hypothermia and Its Risk Factors in Patients Undergoing General Anesthesia in Beijing: A Prospective Regional Survey. PLoS One. 2015 Sep 11;10(9):e0136136. doi: 10.1371/journal.pone.0136136. eCollection 2015. — View Citation
Yi J, Zhan L, Lei Y, Xu S, Si Y, Li S, Xia Z, Shi Y, Gu X, Yu J, Xu G, Gu E, Yu Y, Chen Y, Jia H, Wang Y, Wang X, Chai X, Jin X, Chen J, Xu M, Xiong J, Wang G, Lu K, Yu W, Lei W, Qin Z, Xiang J, Li L, Yao M, Huang Y. Establishment and Validation of a Pred — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of intraoperative hypothermia | Core temperature<36? | During operation | |
Secondary | The amount of Intraoperative blood loss/blood transfusion | During operation | ||
Secondary | Length of stay in PACU | Postoperative during in postanaesthesia care unit, up to 24 hours after surgery | ||
Secondary | The incidence of Surgical site infection | WIthin 30 days postoperative | ||
Secondary | Lenght of Stay in hospital | impatient period, up to 6 month after surgery | ||
Secondary | Lenght of Stay in ICU | impatient period, up to 6 month after surgery | ||
Secondary | Incidence of Adverse cardiovascular events | WIthin 6 month post operation | ||
Secondary | Incidence of shiver | during in postanaesthesia care unit, up to 24 hours after surgery | ||
Secondary | Mini-Mental State Examination (MMSE), | It's a scare to evaluate cognitive function. Total score is 30 . Higher values represent a better cognitive function. | One day preoperation and 1 , 7,30 days postoperation | |
Secondary | digit symbol substitution test | The digit symbol substitution test is an evaluation tool used to assess cognitive functioning. It initially was part of the Wechsler Adult Intelligence Test (WAIS), a well-known test that measures an individual's attention. lower digit symbol test scores were correlated with a higher risk of developing dementia in both the five and 10 year groups.Higher values represent a better cognitive function. | One day preoperation and 1 , 7,30 days postoperation | |
Secondary | Auditory Verbal Learning Test, | a memory test that involves learning verbal material, usually single words presented in a list, that is continually presented over repeated trials. Higher values represent a better memory functions. | One day preoperation and 1 , 7,30 days postoperation | |
Secondary | Color Word Stroop Test | The Stroop Colour and Word Test (SCWT) is a neuropsychological test extensively used to assess the ability to inhibit cognitive interference that occurs when the processing of a specific stimulus feature impedes the simultaneous processing of a second stimulus attribute, well-known as the Stroop Effect. Higher values represent a better ability to inhibit cognitive interference. | One day preoperation and 1 , 7,30 days postoperation | |
Secondary | digit span test. | a memory test that involves remember a series of numbers test short time memory Higher values represent a better memory functions. | One day preoperation and 1 , 7,30 days postoperation | |
Secondary | postoperative cognitive dysfunction incidence | Z score=(postoperative score-preoperative core)/SD of non-surgical group Two or more than two item in cognitive examination Z score<-1.96 Z score=(postoperative score-preoperative core)/SD of non-surgical group Two or more than two item in cognitive examination Z score<-1.96 |
One day preoperation and 1 , 7,30 days postoperation |
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