Post-Mastectomy Chronic Pain Syndrome Clinical Trial
Official title:
Radiofrequency Thoracic Sympathectomy for Chronic Postmastectomy Pain; Randomized Placebo Controlled Study
Verified date | July 2019 |
Source | Assiut University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Postmastectomy pain syndrome (PMPS) is a neuropathic pain that can follow surgical treatment for breast cancer, The antineuropathic medications (antidepressants and anticonvulsants) are disappointing and have low success rate. Continues Radiofrequency lesioning has been reported as treatment for several chronic pain conditions.The concept that the clinical effect of RF was caused by formation of heat had not been challenged. Thermocoagulation of nerve fibers would interfere with the conduction of nociceptive stimuli and pain would be relived. Thoracic sympathectomy has been done for many painful conditions that includes complex regional pain syndrome .It offers the benefit over stellate ganglion block as it blocks the Kuntz fibers that connect to the brachial plexus roots without passing through stellate ganglion.
Status | Completed |
Enrollment | 70 |
Est. completion date | January 1, 2020 |
Est. primary completion date | January 1, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Patients with chronic post-mastectomy pain for at least 6 month post-operative - Patients with VAS = 5 - Patients on pregabalin dose = 150 mg daily - Patients treated with more than one line of anti-neuropathic drugs [e.g. pregabalin+(tricyclic antidepressants or selective serotonin reuptake inhibitors ) or pregabalin+ tramadole] - Lymphedema of the upper limb Exclusion Criteria: - Patient refusal - Coagulopathy - Chest and back deformity hindering procedure impossible - Infection at the introduction site of the needle |
Country | Name | City | State |
---|---|---|---|
Egypt | Madona Misheal Boshra Noman | Assiut |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Egypt,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The intensity of pain | The intensity of pain measured by visual analogue score | up to 3 months after the procedure | |
Secondary | The changes in analgesics consumption | The changes in analgesics consumption | 1 month, 2 month and 3 month post-procedure | |
Secondary | The changes in mid-arm circumference | The changes in mid-arm circumference | 1 month post- procedure | |
Secondary | The changes in post-menopausal hot flashes if it was a pre-procedure complaint | The changes in post-menopausal hot flashes if it was a pre-procedure complaint | 3 month post- procedure |
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