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Study on cardio-cerebral protection of dexmedetomidine combined with shenmai injection in patients undergoing cardiovascular surgery under cardiopulmonary bypass

Study on cardio-cerebral protection of dexmedetomidine combined with shenmai injection in patients undergoing cardiovascular surgery under cardiopulmonary bypass

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087036
Enrollment
Unknown
Registered
2024-07-17
Start date
2022-06-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Heart disease

Interventions

Control group (Group C):0.9% sodium chloride injection intravenous micropump
Dexmedetomidine Group (Group D):10 minutes before anesthesia induction, a micropump was used to pump continuously at a rate of 0.4 µg·kg-1·h-1 until the end of the operation
Shenmai injection group (S group):After 10 minutes of successful anesthesia-induced intubation and at the beginning of the transfer, 0.6 mL/kg Shenmai injection (Dali Pharmaceutical Co., Ltd., 10ml/tu
Dexmedetomidine + Shenmai injection group (DS group):10 minutes before anesthesia induction, a micropump pump was used to pump continuously at a rate of 0.4 µg·kg-1·h-1 until the end of the operation.

Sponsors

Guangxi Zhuang Autonomous Region People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1: Inclusion criteria: (1) informed consent of patients and families; (2) Age> 60 years old; (3) ASA is graded at Class II or III; (4) NYHA is graded as Class II or III; (5) For cardiac patients who undergo elective cardiovascular surgery, the left ventricular ejection fraction EF=45%; (6) No myocardial infarction in the past 3 months; (7) There was no severe heart failure and malignant arrhythmia in the past, and no hyperglycemia and hypertension that were difficult to control; (8) No severe hearing and visual impairment.

Exclusion criteria

Exclusion criteria: 1: Exclusion criteria: (1) preoperative cognitive impairment or mental illness and inability to communicate; (2) Those who have adverse reactions to ginseng injection; (3) Those with severe liver, kidney, lung and brain dysfunction before surgery; (4) the presence of sinus bradycardia and atrioventricular block of any level before surgery; (5) There was an allergic phenomenon to the relevant anesthetic drugs and experimental drugs involved in this study, as well as a history of severe plasma allergy; (6) Those who have recently used traditional Chinese medicine treatment.

Design outcomes

Primary

MeasureTime frame
WBC;N%;HMGB1;hs-CRP;CK-MB;cTnI;NSE;S100ß;MMSE;CAM;SCL-90;

Countries

China

Contacts

Public ContactGongZheng

Guangxi Zhuang Autonomous Region People's Hospital

278387381@qq.com+86 133 6761 7092

Outcome results

None listed

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