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Clinical Research on Auricular Acupoint Bean Implantation Combined with Nasal Spray of Dexmedetomidine for Perioperative Sleep Management in Knee Arthroscopy Surgery

Clinical Research on Auricular Acupoint Bean Implantation Combined with Nasal Spray of Dexmedetomidine for Perioperative Sleep Management in Knee Arthroscopy Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125444
Enrollment
Unknown
Registered
2026-05-27
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Perioperative sleep disorders

Interventions

Auricular point bean embedding therapy group (Group A):The treatment for Group A lasted for 5 days, from the day before surgery to the third day after surgery. Before the procedure, 75% ethanol was us
Nasal spray dexmedetomidine treatment group (Group B):Patients in Group B received nasal spray dexmedetomidine treatment (2.5ug/kg) 5 minutes before going to bed every night for a total of 5 days, spa
Auricular point embedding combined with nasal spray of dexmedetomidine treatment group (Group C):Patients in Group C received auricular point embedding therapy during the same time period (from the da

Sponsors

Ganzhou Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are scheduled to undergo knee arthroscopy under general anesthesia; 2. Preoperative Insomnia Severity Index (ISI) score > 7; 3. Aged between 18 and 65, with no gender restrictions; 4. ASA classification is from I to III; 5. Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. The duration of the surgery is less than 1 hour or greater than 3 hours; 2. The ear exhibits inflammation, damage, eczema, or chilblain; 3. Presence of intranasal lesions or abnormalities in nasal cavity structure; 4. Confirmed or suspected to have Obstructive Sleep Apnea Syndrome; 5. Heart Rate (HR) < 60 beats per minute, or suffering from sick sinus syndrome, or having second-degree or higher-degree atrioventricular block without an implanted cardiac pacemaker; 6. Suffering from severe comorbidities or mental disorders; 7. Existence of alcohol or drug dependency; 8. Being in the gestation period, lactation period, or planning to get pregnant in the near future; 9. Unable to communicate effectively or refuse to cooperate with treatment.

Design outcomes

Primary

MeasureTime frame
Objective sleep indicators;Subjective sleep indicators;Restoration quality;—

Countries

China

Contacts

Public ContactYang Wenyi

Ganzhou Traditional Chinese Medicine Hospital

2496700057@qq.com+86 159 4699 7288

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026