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Clinical observation of ultrasound guided stellate ganglion block in the treatment of postoperative sleep disorders

Clinical observation of ultrasound guided stellate ganglion block in the treatment of postoperative sleep disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070330
Enrollment
Unknown
Registered
2023-04-10
Start date
2023-04-10
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Perioperative sleep disorders

Interventions

1:none
2:Stellate ganglion block with 1% lidocaine 4ml
3:Stellate ganglion block with 2% lidocaine 4ml

Sponsors

Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: There are 120 patients with oral and maxillofacial surgery under general anesthesia and tracheal intubation, regardless of gender, aged 18-40 years, with ASA grade I or II. Stay at AICU for the first night after surgery.

Exclusion criteria

Exclusion criteria: History of other systemic diseases such as congenital heart disease, hypertension, and epilepsy during surgery is excluded. Patients with cervical foreign bodies, coagulation disorders, cervical spondylosis, severe sleep apnea syndrome, respiratory foreign bodies, tumors, polyps, abscesses, and upper respiratory tract infections in the past 2 weeks were excluded. Patients with hearing and speech impairment who are unable to cooperate and refuse to be included in the group.

Design outcomes

Primary

MeasureTime frame
Richards–Campbell Sleep Questionnaire (RCSQ);

Secondary

MeasureTime frame
VAS:VisualAnaloguScale;Complications of nerve block;

Countries

China

Contacts

Public ContactWang Ye

Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

wangyedeemail@126.com+86 158 0159 7504

Outcome results

None listed

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