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Different duration of Valsalva operation for HIFU ablation of liver tumors Effects on brain function in patients

Different duration of Valsalva operation for HIFU ablation of liver tumors Effects on brain function in patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092477
Enrollment
Unknown
Registered
2024-11-18
Start date
2024-11-22
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Burst suppression

Interventions

Short-term VM group:Valsalva maneuver
Control group:No operation is performed
Long-term VM group:Valsalva maneuver

Sponsors

The 2nd Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Patients undergoing HIFU ablation for liver tumor; 2.General anesthesia is required during the operation; 3.American Society of Anesthesiologists (ASA) Physical condition grades I - III; 4.Participate voluntarily and be able to understand and sign informed consent; 5.Patients aged 18-85 years;

Exclusion criteria

Exclusion criteria: 1.Patients with stroke, cerebral hemorrhage, immune system disorders or neurological disorders; 2.Patients with preoperative MMSE = 23; 3.Patients taking drugs that affect the central nervous system; 4.Patients with preoperative pneumothorax, pulmonary bullosa, and underlying respiratory diseases; 5.Patients who are expected to have difficulty managing the airway; 6.Acute coronary syndrome, sinus bradycardia (heart rate 28 kg/m2); 8.Patients with stage 4 or 5 chronic kidney disease; 9.Patients who are expected to require mechanical ventilation after surgery; 10.Hearing, intellectual, communication, cognitive disabilities; 11.For any reason, they could not be included in the study or the researchers considered it inappropriate to include the study; 12.Patients who are expected to be transferred to the ICU after surgery;

Design outcomes

Primary

MeasureTime frame
EEG data (PSD, ApEn, SaEn, PeEn, CFC);Burst suppression;

Secondary

MeasureTime frame
Emergence agitation;Delirium;Postoperative recovery quality;Intraoperative vital signs (SpO2, heart rate, blood pressure);

Countries

China

Contacts

Public ContactShiyu Shu

The 2nd Affiliated Hospital of Chongqing Medical University

745608949@qq.com+86 13527348105

Outcome results

None listed

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