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The impact of anesthesia depth monitoring combined with main dominant frequency and duration of suppression on postoperative agitation and early postoperative recovery quality in elderly patients

The impact of anesthesia depth monitoring combined with main dominant frequency and duration of suppression on postoperative agitation and early postoperative recovery quality in elderly patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125904
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Postoperative Delirium in Elderly Patients:Postoperative delirium in elderly patients is a common acute brain dysfunction syndrome following surgery. It is characterized by an acute and transient alteration in cognitive function occurring within the first week after surgery (particularly within 24 to 72 hours). Its core features include:1.Acute Onset: Symptoms appear suddenly.2.Fluctuating Course:

Interventions

Routine Clinical Monitoring Group:Anesthetic dosages were adjusted by experienced anesthesiologists based on traditional parameters such as heart rate, blood pressure, and oxygen satur
Depth of Anesthesia Monitoring Group:Anesthetic dosage was adjusted based on vital signs and the Ai parameter monitored in real-time by the ConView system to maintain stable anesthesia de

Sponsors

The Second Affiliated Hospital of Inner Mongolia University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 65 and 80 years; 2.Scheduled for elective surgery (with an estimated duration of 1 to 3 hours); 3.American Society of Anesthesiologists (ASA) physical status I–II; 4.Informed consent obtained and signed by family members; 5.Preoperative fasting for more than 8 hours, with no administration of premedication (e.g., sedatives, analgesics, etc.).

Exclusion criteria

Exclusion criteria: 1.Concomitant neurological diseases (e.g., epilepsy, cerebral palsy, cognitive impairment, etc.); 2.Severe insufficiency of cardiac, pulmonary, hepatic, or renal function; 3.Uncorrected electrolyte disturbances or acid-base imbalance; 4.Allergy to anesthetic agents used in this study; 5.Poor skin condition precluding the application of EEG electrodes; 6.High surgical urgency requiring rapid sequence induction of anesthesia; 7.Inability of the patient and family to cooperate with postoperative assessments; 8.Participation in other clinical drug trials within the past 3 months; 9.Patients deemed unsuitable for participation in this trial by the investigator.

Design outcomes

Primary

MeasureTime frame
Early postoperative recovery indicators;Electroencephalographic parameters;Incidence and severity of postoperative delirium;

Countries

China

Contacts

Public ContactWang Xiao Dong

The Second Affiliated Hospital of Inner Mongolia University

wxd-o@163.com+86 471 2575888

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026