Overview

US-guided Sciatic Nerve Block: Evaluation of the Intraneural Ropivacaine Minimal Effective Volume (MEV90)

Status:
Completed
Trial end date:
2017-04-01
Target enrollment:
0
Participant gender:
All
Summary
This prospective, double-blinded study evaluates intraneural ropivacaine 1% Minimal Effective Volume (MEV90) for ultrasound-guided (US) popliteal sciatic nerve block, with Up-and-down methodology. To evaluate any neurological complications, an electrophysiological assessment will also be performed preoperatively and at 5 weeks after surgery.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
ASST Gaetano Pini-CTO
Treatments:
Ropivacaine
Criteria
Inclusion Criteria:

- Age above 18 years old

- ASA I-III

- Signed informed consensus

Exclusion Criteria:

- ASA IV

- Unstable neurological disease

- DM type I-II

- Allergy to ropivacaine-mepivacaine

- Opioid chronic treatment

- Consensus refusal or not valid

- Rheumatoid arthritis

- Baseline electrophysiological study positive finding

- Postoperative intensive care required