Clinical Trials Directory

Trials / Completed

CompletedNCT01376960

Ankle Block Versus Popliteal Fossa Block as Primary Anesthesia for Forefoot Surgical Procedures

Ankle Block Versus Popliteal Fossa Block as Primary Anesthesia for Forefoot Surgical Procedures: A Prospective Comparison

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
202 (actual)
Sponsor
OrthoCarolina Research Institute, Inc. · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare, for the first time ever, single shot popliteal fossa blocks to ankle blocks as primary anesthesia for patients undergoing forefoot procedures. The primary outcome variable for this study is the percentage of patients that convert to general anesthesia following either a single shot popliteal fossa block or ankle block. H0: There is no difference in the percentage of patients that convert to general anesthesia between single shot popliteal fossa blocks and ankle blocks. HA: There will be a lower percentage of patients receiving a single shot popliteal fossa block that convert to general anesthesia compared to patients receiving an ankle block.

Conditions

Interventions

TypeNameDescription
PROCEDUREelective forefoot surgeryIncludes both soft-tissue and osseous procedures.

Timeline

Start date
2011-06-01
Primary completion
2015-01-01
Completion
2016-07-01
First posted
2011-06-20
Last updated
2016-08-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01376960. Inclusion in this directory is not an endorsement.