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Effects of Preoperative Ultrasound-Guided Right Stellate Ganglion Block on Postoperative Quality of Recovery in Patients undergoing Gynecological Laparoscopic Surgery: A Prospective Randomized Controlled Clinical Trial

Effects of Preoperative Ultrasound-Guided Right Stellate Ganglion Block on Postoperative Quality of Recovery in Patients undergoing Gynecological Laparoscopic Surgery: A Prospective Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078762
Enrollment
Unknown
Registered
2023-12-18
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Gynecological benign tumor

Interventions

Test group:Ultrasound-guided right stellate ganglion block
Control group:Blank control

Sponsors

Yan‘an Hospital of Kunming City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. 18-65 years old, BMI 18~27 kg/m^2; 2.Patients undergoing elective laparoscopic resection of benign tumors; 3.ASA II-III.

Exclusion criteria

Exclusion criteria: 1.Allergic to the drug used in the study; 2.Patients with moderate to severe heart and lung disease, liver and kidney disease, cerebrovascular disease, malignant conduction block, sinus bradycardia, and diabetes; 3. There are neurological, mental system or mental illness can not cooperate, can not understand the content of the scale; 4. Coagulation dysfunction; 5. Serious systemic infection or an infected person at the puncture site; 6.Smoking and alcohol dependence; 7. Pregnant women.

Design outcomes

Primary

MeasureTime frame
40-item Quality of Recovery (QoR-40);

Secondary

MeasureTime frame
Athens Insomnia Scale score;Postoperative gastrointestinal function recovery;Postoperative pain;

Countries

China

Contacts

Public ContactWuming Bu

Yan‘an Hospital of Kunming City

13577030908@163.com+86 135 7703 0908

Outcome results

None listed

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