Efficacy of Ultrasound-assisted Caudal Epidural Pulsed Radiofrequency for Anal Pain in Cancer Patients,
NCT ID: NCT06008899
Last Updated: 2024-08-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
40 participants
INTERVENTIONAL
2023-08-25
2025-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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ultrasound (US) assisted caudal epidural pulsed radiofrequency
US assisted caudal epidural pulsed radiofrequency
patients will receive US assisted caudal epidural pulsed radiofrequency and followed up to 8 weeks
conventional medical treatment
No interventions assigned to this group
Interventions
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US assisted caudal epidural pulsed radiofrequency
patients will receive US assisted caudal epidural pulsed radiofrequency and followed up to 8 weeks
Eligibility Criteria
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Inclusion Criteria
* cancer-related anal or perineal pain
Exclusion Criteria
* allergies to the contrast dye
* patients with moderate or significant cardiac/respiratory disease or hepatic
18 Years
60 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Fatma Adel El sherif,MD
associate professor of anesthesia, intensive care and pain management
Locations
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South Egypt Cancer instIitute
Asyut, , Egypt
Countries
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Facility Contacts
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Other Identifiers
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629
Identifier Type: -
Identifier Source: org_study_id
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