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Analysis of the correlation between perioperative blood glucose and delirium in elderly patients with coronary artery bypass grafting and the study of acupoint intervention

Analysis of the correlation between perioperative blood glucose and delirium in elderly patients with coronary artery bypass grafting and the study of acupoint intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000500
Enrollment
Unknown
Registered
2025-03-10
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Coronary heart disease

Interventions

Experimental group:Transcutaneous electrical acupoint stimulation combined with auricular acupoint pressure intervention programme on the basis of routine blood glucose management in the control group
Control group:Implementation of a routine blood glucose management programme

Sponsors

Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) between 60 and 85 years of age; (2) elective coronary artery bypass grafting under extracorporeal circulation.

Exclusion criteria

Exclusion criteria: (1) have a history of mental illness or mild cognitive impairment (score <3 using Mini-Cog screening); (2) have a history of alcoholism or history of substance abuse; (3) have severe vision hearing and speech impairments; (4) require long-term use of hormonal medications; (5) contraindications to transcutaneous electrical acupoint stimulation or auricular acupressure: e.g. pacemaker skin infection auricular skin damage allergy to polar tablets etc.; (6) the existence of severe liver and kidney dysfunction before the operation; (7) the existence of obvious blood sugar abnormalities before the operation such as HbA1c = 6.5%; (8) the number of days between confirmation of surgery and the day of surgery is less than 3 days; (9) already participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Incidence of delirium at 7 days postoperatively;

Secondary

MeasureTime frame
Duration of mechanical ventilation;Intensive Care Unit Hospitalization Days;Dosage of postoperative insulin;postoperative anxiety;Coefficient of variation of blood glucose at 3 days postoperatively;Blood glucose 1 day before surgery;Neutrophil to lymphocyte ratio on the first postoperative day;C-reactive protein level on the first postoperative day;postoperative pain;Incidence of abnormal blood glucose values at 3 days postoperatively;

Countries

China

Contacts

Public ContactLin Yanjuan

Fujian Medical University Union Hospital

fjxhyjl@163.com+86 591 8621 8336

Outcome results

None listed

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