Efficacy of Ultrasound-assisted Caudal Epidural Pulsed Radiofrequency for Anal Pain in Cancer Patients,
Recruiting
N/A
Interventional Study
Perineal Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 60
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 40 (estimated)
- Sponsor
- Assiut University · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* American Society of Anesthesiology physical status of I or III (ASA), of both sex
* cancer-related anal or perineal pain
Exclusion Criteria:
* coagulopathies
* allergies to the contrast dye
* patients with moderate or significant cardiac/respiratory disease or hepatic
Contacts
No contact information available.