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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ChiCTR
Last refreshed on: 24 January 2022
Main ID:  ChiCTR1900027197
Date of registration: 2019-11-04
Prospective Registration: No
Primary sponsor: The First Affiliated Hospital of Zhengzhou University
Public title: Study on the protective effect of desflurane combined with propofol on the brain of patients with moyamoya disease undergoing cerebral revascularization
Scientific title: Study for the protective effect of desflurane on the brain of patients with moyamoya disease
Date of first enrolment: 2019-05-01
Target sample size: Group D:30;GroupP:30;GroupPD:30;
Recruitment status: Completed
URL:  http://www.chictr.org.cn/showproj.aspx?proj=44942
Study type:  Interventional study
Study design:  Parallel  
Phase:  4
Countries of recruitment
China
Contacts
Name: Wang Zhongyu   
Address:  1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, China 450052
Telephone: +86 13937165514
Email: wzy781217@163.com
Affiliation:  The First Affiliated Hospital of Zhengzhou University
Name: Feng Fengxi   
Address:  1 Jianshe Road East, Erqi District, Zhengzhou, He'nan, China 450052
Telephone: +86 13849030473
Email: 756023673@qq.com
Affiliation:  The First Affiliated Hospital of Zhengzhou University
Key inclusion & exclusion criteria
Inclusion criteria: Aged 20-65 years; BMI 18-25kg/m2; ASA I-II grade; patients without hypertension or with hypertension history and satisfactory blood pressure control; patients without diabetes or with diabetes history and satisfactory blood glucose control.Hemoglobin (HB) >= 100g / L, hematocrit (HCT) >= 30%; no coagulation dysfunction, no long-term history of antidepressant and analgesic drugs
Exclusion criteria: Patient or his family refused to sign the informed consent form and patients with liver and kidney function abnormality, lung function abnormality, serious coronary heart disease, serious endocrine disease, mental disease, drug abuse, coagulation function abnormality, unconsciousness, organ intubation difficulty, and severe fluctuation of hemodynamics during operation.

Age minimum: 20
Age maximum: 65
Gender: Both
Health Condition(s) or Problem(s) studied
Moyamoya disease
Intervention(s)
Group D:Desflurane for anesthesia maintenance;GroupP:Propofol;GroupPD:Desflurane and propofol;
Primary Outcome(s)
Artefiovenous oxygen content difference;Cerebral oxygen extraction rate;Jugular venous blood oxygen saturation;Complication;GluERMB;LacPR;LOI;mRS score;NSE;S100ß protein;
Secondary Outcome(s)
Mean arterial pressure;
Secondary ID(s)
Source(s) of Monetary Support
self-financing
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 26/04/2019
Contact:
Tian Li
Results
Results available:
Date Posted:
Date Completed:
URL:
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