Status:
UNKNOWN
Combining Stellate Ganglion and T2 and T3 Radiofrequency Ablation on Post-mastectomy Complex Regional Pain Syndrome
Lead Sponsor:
National Cancer Institute, Egypt
Conditions:
Stellate Ganglion
Radiofrequency Ablation
Eligibility:
FEMALE
18-60 years
Phase:
NA
Brief Summary
The aim of this study is to evaluate the efficacy of the combination of Ultra Sound (US) guided radiofrequency stellate ganglion block (SGB) and radiofrequency Thoracic Paravertebral block (TPVB) comp...
Detailed Description
Breast cancer is the most common malignancy among females, with an incidence of about 2.1 million women each year. It is the most common cause of cancer-related deaths among women. Modified Radical Ma...
Eligibility Criteria
Inclusion
- Female patients.
- Type of surgery: Modified Radical Mastectomy MRM.
- Physical status ASA II, III.
- Duration of more than 6 months and less than 2 years.
- Moderate and severe pain (visual analog scale \[VAS\] ≥ 40 mm).
- Pain described as a refractory to strong opioids (oxycodone) and adjuvant therapy such as(pregabalin) for which more invasive interventions could be tried.
Exclusion
- Patient refusal.
- Patient with local and systemic sepsis.
- Local anatomical distortion.
- History of contralateral chest disease or pneumonectomy.
- Known sensitivity or contraindication to the drug used in the study.
- History of psychological disorders.
- Contraindication to regional anesthesia, e.g., pre-existing peripheral neuropathies and coagulopathy.
- Severe respiratory or cardiac disorders. Advanced liver or kidney disease.
- Pregnancy.
- Physical status ASA IV and Male patients.
Key Trial Info
Start Date :
October 7 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 15 2024
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT06033456
Start Date
October 7 2023
End Date
March 15 2024
Last Update
October 10 2023
Active Locations (1)
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1
National Cancer Institute
Cairo, Egypt, 11796