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The Effect of Ultrasound-guided Stellate Ganglion Block on Postoperative Sleep Quality in Patients Undergoing Thyroidectomy: A Randomized Controlled Trial

The Effect of Ultrasound-guided Stellate Ganglion Block on Postoperative Sleep Quality in Patients Undergoing Thyroidectomy: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106958
Enrollment
Unknown
Registered
2025-07-31
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Postoperative sleep disorder

Interventions

Control group:- In the control group, ultrasound-guided localization of the stellate ganglion was performed before induction, but no invasive procedures were carrie
Intervention group:Stellate ganglion block (SGB)

Sponsors

First Affiliated Hospital of Gannan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years old, BMI 18.5-24 kg/m^2; - ASA classification grade I-II. 2.Patients scheduled for elective thyroidectomy under general anesthesia. 3.Patients who voluntarily signed the relevant informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe hepatic and renal dysfunction or lung injury; abnormal coagulation function; 2. Patients with a history of obstructive sleep apnea syndrome; 3. Alcohol or drug dependence; 4. Use of psychotropic drugs within two weeks prior to enrollment; 5. Dementia or obvious neurological diseases (such as stroke, epilepsy, intracranial tumor, history of Parkinson's disease, etc.); 6. Inability to understand the questionnaires used in the study, or severe visual impairment; 7. Participation in other clinical trials; 8. Preoperative PSQI score =7 or existing sleep disorders; 9. Known allergy to any drugs used in the study.

Design outcomes

Primary

MeasureTime frame
Leeds Sleep Evaluation Questionnaire (LSEQ);Sleep satisfaction evaluation;Total sleep time on the first postoperative night;

Secondary

MeasureTime frame
Inflammation-related indicators;Visual Analogue Scale (VAS) for pain;Hemodynamic changes;Incidence of postoperative nausea and vomiting, sore throat;

Countries

China

Contacts

Public ContactWeidong Liang

First Affiliated Hospital of Gannan Medical University

lwd0929@gmu.edu.cn+86 797 868 9034

Outcome results

None listed

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