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The effect of repetitive transcranial magnetic stimulation on postoperative sleep disorders in patients undergoing thoracoscopic lung resection: A prospective,single-center, randomized controlled trial

The effect of repetitive transcranial magnetic stimulation on postoperative sleep disorders in patients undergoing thoracoscopic lung resection: A prospective, single-center, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128992
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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. Age >= 18 years old, gender not restricted; 2. Intending to undergo elective thoracoscopic lung resection (including lobectomy, segmentectomy or wedge resection) under general anesthesia; 3. American Society of Anesthesiologists (ASA) classification I - III; 4. Normal preoperative cognitive function (Mini-Mental State Examination MMSE score >= 24 points); 5. Normal language communication and comprehension ability, able to cooperate in completing self-assessment scales; 6. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with a preoperative Pittsburgh Sleep Quality Index (PSQI) score greater than 7, or those already having sleep disorders such as sleep apnea syndrome, narcolepsy, etc.; 2. Patients who have been taking sedative-hypnotic drugs, antidepressants or opioid drugs for more than 3 months before the surgery; 3. Patients with contraindications for rTMS (such as a history of epilepsy, intracranial metal implants, cardiac pacemakers); 4. Patients with severe mental disorders or cognitive dysfunction; 5. Patients who have participated in other studies or whose family members or patients have refused to participate in this study.

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative sleep disorder (PSD);

Secondary

MeasureTime frame
Frailty score;Postoperative dosage of opioid drugs;Anxiety score;Postoperative objective sleep indicators;Overall quality of postoperative recovery;Incidence of postoperative delirium (POD);Postoperative pain scores at rest and on movement;

Countries

China

Contacts

Public ContactHuadong Ni

The First Hospital Of Jiaxing

huadongni@126.com+86 15068386387

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026