Clinical Trials Directory

Trials / Completed

CompletedNCT01445249

Medial Forefoot Block for Analgesia After Foot Surgery

A Randomised, Blinded Comparison of a Nerve Stimulator Guided Ankle Block Compared to a Landmark Guided Ankle Block for Pain Relief After Forefoot Surgery.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Hull University Teaching Hospitals NHS Trust · Other Government
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Forefoot surgery includes bunion surgery and similar reconstructive bone cutting surgery and is very painful. Local anaesthetic nerve blocks are used to provide pain relief after this work. The purpose of this study is to compare two techniques: one using anatomical landmarks alone to guide local anaesthetic infiltration, the other using peripheral nerve stimulation to guide local anaesthetic infiltration (termed medial forefoot block). The two techniques will be compared for reliability of postoperative analgesia.

Detailed description

More extensive description not desired.

Conditions

Interventions

TypeNameDescription
PROCEDURELandmark guided ankle block.25-30mls 0.5% levobupivacaine will be infiltrated to provide a landmark guided ankle block.
PROCEDUREPNS guided block.This group will have 25-30mls of 0.5% levobupivacaine infiltrated as directed by peripheral nerve stimulation.

Timeline

Start date
2007-03-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2011-10-03
Last updated
2019-07-15

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT01445249. Inclusion in this directory is not an endorsement.