Nervous decompression
Conditions
Interventions
The study will include 200 patients with clinical suspicion of intrapelvic nerve compression treated at the Pelvic Neurodisfunctions Clinic of the Department of Gynecology at UNIFESP and in a private
M54.3
Sponsors
UNIFESP
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with clinical suspicion of intrapelvic nerve compression;over 18 years
Exclusion criteria
Exclusion criteria: Adolescents under the age of 18;pregnant women;patients with cognitive limitations
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Brazil
Contacts
Public ContactGustavo Fernandes
Outcome results
None listed