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A study of the effect of a subanesthetic dose of esketamine on intraoperative burst suppression in general anesthesia in elderly debilitated patients

A study of the effect of a subanesthetic dose of esketamine on intraoperative burst suppression in general anesthesia in elderly debilitated patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091042
Enrollment
Unknown
Registered
2024-10-19
Start date
2024-03-15
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

burst suppression and postoperative cognitive function

Interventions

Control group:0.9% Sodium Chloride solution

Sponsors

Anhui NO.2 Provincial People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age range of 60-85 years old; 2.BMI:18.5-27.0; 3.ASA grades I-III and cardiac function grades I-II; 4. Patients with normal liver and kidney function, and patients with normal coagulation function; 5. Fully understand the purpose and significance of this trial, as well as the voluntary signing of informed consent by the patient's family members.

Exclusion criteria

Exclusion criteria: 1. Patients with neurological disorders and those taking psychiatric medications 2. Patients with severe hypertension, intracranial hypertension, high intraocular pressure, and a history of cerebrovascular accidents 3. Patients with hyperthyroidism and adrenal pheochromocytoma 4. Patients with heart dysfunction, history of coronary artery disease, cardiomyopathy, or angina pectoris 5. Determine/suspect the abuse or long-term use of anesthetic sedatives and analgesics; Contraindications for the use of ketamine

Design outcomes

Primary

MeasureTime frame
The incidence and frequency of burst suppression ;Postoperative cognitive function;

Secondary

MeasureTime frame
PSI value of anesthesia depth at each time point;Visual simulation pain score and number of analgesic pump presses within 48 hours after surgery;

Countries

China

Contacts

Public ContactWang Yiqiao

Anhui No.2 Provincial People’s Hospital

309734607@qq.com+86 158 5694 0528

Outcome results

None listed

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