Skip to content

Effect of Transcutaneous Vagus Nerve Stimulation on Perioperative Sleep Quality in Patients Undergoing Thyroidectomy

Effect of Transcutaneous Vagus Nerve Stimulation on Perioperative Sleep Quality in Patients Undergoing Thyroidectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118927
Enrollment
Unknown
Registered
2026-02-12
Start date
2026-02-12
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Perioperative sleep quality

Interventions

Experimental Group:placed at the cymba conche of the left ear to stimulate the auricular branch of the vagus nerve
Control Group:Sham stimulation

Sponsors

The Second Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.scheduled to undergo thyroidectomy; 2.ASA physical status I–III; 3.age >=18 years; 4.were all clear-headed, able to communicate fluently, and willing to participate in this research;

Exclusion criteria

Exclusion criteria: 1.Unwillingness to participate; 2.Preoperative Pittsburgh Sleep Quality Index [PSQI] score >=7; 3.History of neurological or psychiatric disorders, psychiatric diseases, or personality abnormalities, such as schizophrenia, depression, epilepsy, Parkinson's disease, multiple sclerosis, etc.; 4.Presence of sleep-related disorders (e.g., obstructive sleep apnea syndrome); 5.Long-term use of sedative-hypnotic medications; 6.History of severe cardiovascular diseases or severe hepatic or renal insufficiency; 7.BMI >= 30 or presence of sleep apnea syndrome; 8.Unrepaired skull defects, or presence of metal or cardiac pacemaker implants. 9.Participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Incidence of PSD on the first day after operation;

Secondary

MeasureTime frame
Incidence of PSD on the third day after operation;Changes in other sleep parameters measured via the AIS;Anxiety and depression scores from the first day to the third day after operation;Postoperative pain scores at rest and during movement at 24 h 48 h and 72 h;The quality of recovery on postoperative days 1 and 3;

Countries

China

Contacts

Public ContactMuhuo Ji

The Second Affiliated Hospital of Nanjing Medical University

jimuhuo2009@sina.com+86 159 9623 5006

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026