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Effect of ultrasound-guided stellate ganglion block on sleep state in patients undergoing supratentorial craniotomy

Effect of ultrasound-guided stellate ganglion block on sleep state in patients undergoing supratentorial craniotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020611
Enrollment
Unknown
Registered
2019-01-10
Start date
2019-02-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

General anesthesia

Interventions

Group S:Stellate ganglion block before anesthesia

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 65 years old male and female; (2) BMI was 18-24kg/m2; (3) ASA I-III grade; (4) Well sleep function; all the patients were assessed with Pittsburgh Sleep quality Index one month before operation; The range of scoring < 7; (5) Can be correctly evaluated; (6) Elective general anesthesia for supratentorial tumor resection patients.

Exclusion criteria

Exclusion criteria: (1) severe cardiovascular and respiratory dysfunction, abnormal liver and kidney function, abnormal central nervous system function; (2) language and intelligence impairment, poor compliance; (3) long-term use of antidepressants or sedatives. (diazepam, tricyclic antidepressants, antihypertensive drugs, glucocorticoids, aminophylline, antihistamines, etc.); (4) allergy to local anesthetics, puncture site infection, and presence of abnormal coagulation; (5) participation in other clinical trials. Testing and refusing to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Pittsburgh Sleep Quality Index;Deep sleep duration / total sleep duration;

Secondary

MeasureTime frame
adverse effects;

Countries

China

Contacts

Public ContactChen Xiuxia

Xuzhou Medical University

cxxlxy@sina.com+86 18052268332

Outcome results

None listed

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