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An anesthetic method to improve the quality of recovery in elderly patients

To study the effect of total intravenous anesthesia before the end of operation on the improvement of recovery quality and postoperative cognitive dysfunction in elderly patients with long-term intravenous-inhalation anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100920
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-04-20
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Postoperative Cognitive Dysfunction

Interventions

Propofol group:Propofol was used instead of sevoflurane before the end of operation
Sevoflurane group:Sevoflurane and remifentanil were used throughout the whole process, and the anesthetic medication management during the maintenance period was the same as that of the propofol group

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
66 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age greater than 65 years old; 2. American Society of Anesthesiologists (ASA) Physical Status I-III; 3. Primary school education or above; 4. Negative bell painting test; 5. MMSE score> 23 points; 6. Operation time>3h; 7. Sign the informed consent form and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1. Age> 85 years; 2. Neurosurgery and cardiac surgery; 3. Patients with a history of neurological diseases, stroke, other significant central nervous system diseases or severe psychiatric diseases, multiple trauma and head trauma, endocrine or metabolic diseases.

Design outcomes

Primary

MeasureTime frame
The score was higher than that of the control group;Blood pressure was stable with little fluctuation;The score was higher than that of the control group;Short time to use;Differences were observed for multiple metabolites;Small changes in heart rate;Short time to use;The incidence of postoperative cognitive dysfunction is low;

Secondary

MeasureTime frame
No shivering;The patient was awake and quietly cooperative;Don't cough;VAS score for analgesia;

Countries

China

Contacts

Public ContactXue Li

The Second Affiliated Hospital of Harbin Medical University

LX84635616@163.com+86 451 8660 5452

Outcome results

None listed

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