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The efficacy of transcranial alternating current stimulation on the quality of postoperative recovery in patients undergoing lumbar fusion surgery

The efficacy of transcranial alternating current stimulation on the quality of postoperative recovery in patients undergoing lumbar fusion surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122565
Enrollment
Unknown
Registered
2026-04-15
Start date
2026-04-18
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Lumbar intervertebral disc protrusion, lumbar spinal canal stenosis and lumbar spondylolisthesis

Interventions

Intervention group:The transcranial alternating current stimulation device will be used 30 minutes before the operation, after extubation on the day of the operation, on the first day after the operat
Control group:The control group will be given the same duration of sham stimulation at the same location.

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18 - 75 years old 2.ASA classification: II - III 3.Right-handed 4.Plan to undergo an elective open approach lumbar fusion surgery involving 1-2 segments caused by lumbar degenerative diseases 5.The anesthesia method is the combined inhalation-intravenous anesthesia via tracheal intubation

Exclusion criteria

Exclusion criteria: 1.The patient refusing to sign the informed consent form 2.Has already participated in another intervention study 3.With neurological or mental disorders or a history of neurological or mental illness in the past 4.With a history of brain or scalp injury or a history of brain surgery 5.Cognitive dysfunction and difficulty in communication 6.Refusing to use the pain relief pump 7.With a metal implant in the body 8.Substance or drug abuse 9.With severe cardiovascular diseases or severe liver or kidney dysfunction 10.With a history of lumbar surgery 11.Any other factors that researchers think might influence the outcome of the study

Design outcomes

Primary

MeasureTime frame
Postoperative quality of recovery;

Secondary

MeasureTime frame
Postoperative quality of recovery;Postoperative sleep quality;Postoperative opioid consumption;Postoperative complications;The patient's satisfaction score for the anesthesia and surgery.;Postoperative Oswestry Disability Index;Postoperative hospital stay duration;Pain score;The time of the first postoperative ambulation;The time of the first rescue analgesic administration after the surgery;The number of postoperative rescue analgesia ;The incidence of postoperative nausea and vomiting;The incidence of postoperative delirium;Postoperative anxiety and depression score;Postoperative inflammatory markers in blood;

Countries

China

Contacts

Public ContactJunli Cao

Affiliated Hospital of Xuzhou Medical University

caojl0310@aliyun.com+86 516 8326 2686

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026