Postoperative Pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Aged 18 to 65 years, of any gender. 2. Patients with clinically and radiologically confirmed partial or complete unilateral upper limb amputation. 3. Capable of comprehending and independently completing all assessment scales. 4. Willing to provide written informed consent voluntarily.
Exclusion criteria
Exclusion criteria: 1.In addition to upper limb amputation, having severe trauma in other regions (such as head, chest/abdomen, spine) or accompanied by severe multiple injuries. 2.History of central or peripheral nervous system diseases such as epilepsy, Parkinson's disease, multiple sclerosis, or stroke. 3.History of schizophrenia, bipolar disorder, major depression, or currently taking antipsychotic medications. 4.History of alcohol, opioid, or other drug abuse, or participation in other drug clinical trials within the recent 3 months. 5.Presence of severe coagulation dysfunction or currently receiving anticoagulant therapy. 6.Local infection or anatomical abnormalities: presence of infection, tumor, or anatomical structural abnormalities at the cervical puncture site, making it unsuitable for stellate ganglion block procedure. 7.Allergy to study medications: history of allergy to local anesthetics used in the study (lidocaine, ropivacaine) or any other components. 8.Female patients who are pregnant or breastfeeding. 9.Unable to complete follow-up and assessments throughout the entire study period (e.g., 3 months) due to various reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Assessment;Adverse Events Associated with Stellate Ganglion Block; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety Score;Sleep Quality;Depression Assessment;Stress Assessment;Functional Assessment of the Affected Limb;Quality of Life Assessment; | — |
Countries
China
Contacts
Affliated hospital of Jining Medical University