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Influence of dexmedetomidine on myocardial injury during perioperative period of abdominal surgery in elderly diabetic patients and screening of risk factors

Influence of dexmedetomidine on myocardial injury during perioperative period of abdominal surgery in elderly diabetic patients and screening of risk factors

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041681
Enrollment
Unknown
Registered
2021-01-01
Start date
2021-01-05
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Diabetes Mellitus

Interventions

Diabetes+Dexmedetomidine:Dexmedetomidine is infused intravenously at the rate of 0.4 ug/kg/h until 30 minutes before the end of the operation.
Diabetes+Control:The control group was injected with normal saline at the same rate as the DD group
Non diabetes+Dexmedetomidine:Dexmedetomidine is infused intravenously at the rate of 0.4 ug/kg/h until 30 minutes before the end of the operation.
Non diabetes+Control:The control group was injected with normal saline at the same rate as the DD group

Sponsors

Shaanxi Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Accord with the diagnostic criteria of diabetes; 2. There was no significant abnormality in blood routine, liver and kidney function, electrolytes, myocardial enzymes and acid-base balance disorder; 3. Fasting blood glucose = 65 and < 80 years; 7. There was no history of chemotherapy and radiotherapy before operation, and no hormone and immune drugs were used.

Exclusion criteria

Exclusion criteria: 1. Serious circulatory, respiratory, digestive and urinary diseases; 2. Drug addicts or drug abusers, and those who are allergic to narcotic drugs; 3. There are contraindications to operation or anesthesia; 4. Serious arrhythmia; 5. Random blood glucose > 11.1mmol/l; 6. Install temporary or permanent pacemaker; 7. Poor compliance; 8. Death or withdrawal from treatment; 9. Mental patients and critically ill patients; 10. Incomplete clinical data can not determine the efficacy and safety.

Design outcomes

Primary

MeasureTime frame
High sensitivity troponin I;

Secondary

MeasureTime frame
Incidence of cardiovascular events during and within 30 days after operation;

Countries

China

Contacts

Public ContactChang Jianhua

Shaanxi Provincial People's Hospital

chang0808@163.com+86 13572088657

Outcome results

None listed

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