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Multidimensional Mechanisms of Stellate Ganglion Block in Regulating Pain Transmission and Improving Quality of Life after Traumatic Upper Limb Amputation

Multidimensional Mechanisms of Stellate Ganglion Block in Regulating Pain Transmission and Improving Quality of Life after Traumatic Upper Limb Amputation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114918
Enrollment
Unknown
Registered
2025-12-18
Start date
2026-02-28
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Postoperative Pain

Interventions

Sponsors

Affliated hospital of Jining Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

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

MeasureTime frame
Pain Assessment;Adverse Events Associated with Stellate Ganglion Block;

Secondary

MeasureTime frame
Anxiety Score;Sleep Quality;Depression Assessment;Stress Assessment;Functional Assessment of the Affected Limb;Quality of Life Assessment;

Countries

China

Contacts

Public ContactXirong Li

Affliated hospital of Jining Medical University

619174227@qq.com+86 537 290 3019

Outcome results

None listed

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