Treatment and diagnosis of Sciatic and Pudental Intrapelvic pai
Not Applicable
- Conditions
- ervous decompressiong55.8
- Registration Number
- RBR-10ybp9vx
- Lead Sponsor
- IFESP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Patients with clinical suspicion of intrapelvic nerve compression;over 18 years
Exclusion Criteria
Adolescents under the age of 18;pregnant women;patients with cognitive limitations
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcomes were pain scores at 1-year follow up. Clinically relevant pain reduction was defined as a more than 50% reduction in Numeric Rating Scale (NRS)
- Secondary Outcome Measures
Name Time Method To evaluate the time of the onset of symptoms, duration of opioid use, entrapment location and etiology, operative time, intraoperative blood loss and perioperative complications.