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Our primary goal will be to investigate the analgesic efficacy of ultrasound (US)-assisted caudal epidural PRF (pulsed radiofrequency)( stimulation in patients with perineal or anal pain cancer patients using (visual analog scale (VAS) scores from 0 to 10 at the baseline (pretreatment), two, four, and eight weeks; secondary outcomes will be the effects on opioid use and total opioid use in the 24 h, quality of life, patient satisfaction and opioid and intervention related side effects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ultrasound (US) assisted caudal epidural pulsed radiofrequency | Active Comparator |
| |
| conventional medical treatment | No Intervention |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| US assisted caudal epidural pulsed radiofrequency | Procedure | patients will receive US assisted caudal epidural pulsed radiofrequency and followed up to 8 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| visual analog scale (VAS) score 4 weeks post-intervention | Our primary goal will be to investigate the analgesic efficacy of ultrasound-assisted caudal epidural PRF stimulation in patients with perineal or anal pain cancer patients using VAS scores from 0 to 10 at the baseline (pretreatment), two, four, and eight weeks | 8 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| South Egypt Cancer instIitute | Recruiting | Asyut | 171516 | Egypt |
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