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Effect of general anesthesia combined with stele ganglion block on sleep outcomes of patients with chronic insomnia after thoracoscopic surgery

Effect of general anesthesia combined with stele ganglion block on sleep outcomes of patients with chronic insomnia after thoracoscopic surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079356
Enrollment
Unknown
Registered
2024-01-01
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

Perioperative sleep outcome

Interventions

General anesthesia group:The patient underwent routine induction and maintenance of anesthesia until the end of the operation
General anesthesia+Stellate ganglion block group:The patient underwent routine induction and maintenance of anesthesia until the end of the operation,After the surgery, use 5ml of 0.25% ropivacaine fo

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Gender unlimited ? Age 18-75 years old, 18 = BMI = 28Kg/? ? ASA Level I-III ? Patients who require thoracoscopic lobectomy (including partial lobectomy and segmental resection) and are hospitalized ? Having basic reading and comprehension skills, or clear Q&A skills, able to complete scale surveys with the help of medical staff. ? Sign an informed consent form, voluntarily participate in this project and be able to complete it as requiredClose monitoring of patients

Exclusion criteria

Exclusion criteria: ? Existence of mental disorders such as anxiety and depression, as well as other neurological disorders ? Patients with planetary ganglion block, including coagulation dysfunction, local skin infection, thyroid enlargement, and abnormal cardiac excitation conduction, are prohibited ? Patients who are unable to cooperate or persist in treatment, and anticipate poor compliance ? The patient is also participating in other clinical trial studies ? Any researcher deemed unsuitable to participate in this experiment due to other reasons

Design outcomes

Primary

MeasureTime frame
Insomnia Severity Index(ISI));

Secondary

MeasureTime frame
Pittsburgh sleep quality index(PSQI));Self-Rating Scale of Sleep;Deep sleep duration;Light sleep time;Rem sleep time;Visual analog scoring(VAS);The incidence of major postoperative complications;Length of stay(LOS);

Countries

China

Contacts

Public ContactCheng Xinqi

The First Affiliated Hospital of Anhui Medical University

ay_mz_cheng@126.com+86 139 6501 5671

Outcome results

None listed

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