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Transauricular Vagus Nerve Stimulation Improves Postoperative Sleep Disorders in Elderly Patients.

Transauricular Vagus Nerve Stimulation (taVNS) Improves Postoperative Sleep Disorders in Elderly Patients:a Randomized Controlled Study.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06421051
Acronym
Vnstep
Enrollment
164
Registered
2024-05-20
Start date
2024-06-20
Completion date
2025-12-31
Last updated
2025-01-27

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

Conditions

Vagus Nerve Stimulation

Brief summary

Postoperative sleep disorder is one of the common complications after general anesthesia. Compared to patients of various ages, elderly patients have a much higher incidence of postoperative sleep disturbance. Postoperative sleep disorders can have many adverse effects, including cognitive impairment, altered pain perception, and emotional disorders, which are not conducive to the long-term prognosis of elderly patients. Enhancing postoperative sleep quality in older patients has become a significant public health concern in the current day due to its direct relationship to both maximizing surgical outcomes and enhancing physical health. This study intends to conduct a prospective, randomized controlled, triple-blind clinical trial on use of transauricular vagal nerve stimulation to improve sleep disorders in elderly patients after general anesthesia surgery, aiming to investigate the efficacy of transauricular vagal nerve stimulation in postoperative sleep disorders in elderly patients.

Interventions

Transauricular vagal nerve stimulation

Sponsors

Beijing Tiantan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing non-craniocerebral surgery under elective general anesthesia * Age ≥65 years old * American society of Aneshesiologists Grade I to III * Sign informed consent

Exclusion criteria

* Patients who are expected to retain tracheal intubation after surgery * Disturbance of consciousness, mental disorder, inability to cooperate * Expected survival \< 3 months * The estimated operation time is \< 2 hours * The expected postoperative hospital stay is \< 5 days

Design outcomes

Primary

MeasureTime frame
Incidence of sleep disorders within 5 days after surgery.Day 1 to day 5 after surgery.

Secondary

MeasureTime frameDescription
Sleep quality after surgery.Day 1,3,5 after surgery.The investigators collected patient-related information on postoperative days 1, 3, and 5 by using the Pittsburgh Sleep Quality Index (total score ranges from 0 to 21, with higher scores indicating poorer sleep quality) and a sleep monitoring bracelet, and analyzed the subsequent data.
Postoperative pain scoreDay1 and 2 after surgery.The investigators collected information from the patients on the 1st and 2nd postoperative days by Visual Analogue Scale and analyzed the data subsequently. The scale is based on a 10-cm horizontal line drawn on a piece of paper, with 0 cm at one end of the line indicating no pain at all and 10 cm at the other end indicating extreme pain; the level of pain increases from 0 to 10 cm, with higher scores indicating more intense pain. The higher the score, the more severe the pain.

Countries

China

Contacts

Primary ContactRuquan Han, MD
ruquan.han@ccmu.edu.cn8610-59976660

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026