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Comparative study on the efficacy of lidocaine and ropivacaine stastrate ganglion block in insomnia disorder

Comparative study on the efficacy of lidocaine and ropivacaine stastrate ganglion block in insomnia disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098835
Enrollment
Unknown
Registered
2025-03-14
Start date
2025-03-15
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Insomnia

Interventions

0.2% ropivacaine group:0.2% ropivacaine stellar ganglion block + cognitive behavioral therapy
0.8% lidocaine group:0.8% lidocaine stellar ganglion block + cognitive behavioral therapy

Sponsors

The Third Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-75 years old, gender unlimited; 2.It meets the diagnostic criteria of chronic insomnia in the International Classification of Sleep Disorders; 3.Pittsburgh Sleep Quality Index (PSQI) score >=7; 4.Sign an informed consent form with the patient or his family;

Exclusion criteria

Exclusion criteria: 1.Those who are allergic to the drugs (lidocaine, ropivacaine); 2.Patients with consciousness disorder and cognitive dysfunction; 3.Severe heart block or cardiac insufficiency; 4.Abnormal coagulation function, puncture site infection; 5.Patients with other serious organic diseases;

Design outcomes

Primary

MeasureTime frame
Pittsburgh Sleep Quality Index (PSQI);

Secondary

MeasureTime frame
Patient Health Questionnaire-9 (PHQ-9);Generalized Anxiety Disorder Scale (GAD-7);Psychomotor Alertness Test (PVT);Heart rate variability (HRV) test;Sleep diary;Satisfaction with sleep quality;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactWang Yongjia

The Third Affiliated Hospital of Guangzhou University of Chinese Medicine

1258710085@qq.com+86 15963069020

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 19, 2026