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Effect of repetitive transcranial magnetic stimulation on postoperative sleep disorders in patients undergoing open spinal surgery: A single-center, prospective, randomized controlled study

Effect of repetitive transcranial magnetic stimulation on postoperative sleep disorders in patients undergoing open spinal surgery: A single-center, prospective, randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112328
Enrollment
Unknown
Registered
2025-11-12
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

postoperative sleep disturbance

Interventions

Sponsors

The First Hospital Of Jiaxing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective open thoracic or lumbar spine surgery under general anaesthesia with endotracheal intubation; 2. Age >= 18 years; 3. ASA physical status classification <= III; 4. All subjects and their families are willing to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Participants who have already taken part in other studies, or patients and their relatives who refuse to participate in this study; 2. Patients with a preoperative Pittsburgh Sleep Quality Index (PSQI) score >7, or those with pre-existing sleep disorders such as sleep apnoea syndrome or narcolepsy; 3. Body Mass Index (BMI) >=30 kg/m²; 4. Presence of metallic implants in the cranium or heart (e.g., cardiac pacemakers, cochlear implants, cardiac stents); 5. History of neurological or psychiatric disorders; 6. History of cranial or cerebral disease, prior cranial surgery, or cranial/scalp trauma or infection; 7. History of epilepsy or familial predisposition; 8. History of substance dependence or alcohol abuse; 9. Patients transferred to the ICU post-operatively; 10. Pregnancy or lactation; 11. Cognitive impairment or inability to communicate; 12. Allergy to anaesthetic agents or other medications used in this trial.

Design outcomes

Primary

MeasureTime frame
The incidence rate of postoperative sleep disorders;

Secondary

MeasureTime frame
Sleep quality after the operation;Depression score;Postoperative analgesic medication use;Postoperative recovery quality;The incidence of sleep disorders on the 7th day after surgery;Motor pain scores;serological indicators;Rset pain scores;Objective sleep quality;The incidence of delirium;Anxiety score;

Countries

China

Contacts

Public ContactHanqi,Wang

The First Hospital Of Jiaxing

wanghanqi2025@163.com+86 573 82519999

Outcome results

None listed

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