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Popliteal Nerve Block for Postoperative Pain Control in Ankle and Hindfoot Reconstruction

Pain, Postoperative Clinical Trial

Official title:
Popliteal Nerve Block for Postoperative Pain Control in Patients Undergoing Ankle and Hindfoot Reconstruction About the Talus

Clinical Trial Summary

The purpose of this study is to evaluate outcomes of popliteal nerve blocks for postoperative pain control in patients undergoing ankle and hindfoot reconstruction surgeries. The following outcomes will be analyzed: length of hospital stay, level of pain control, pain medication use, complications, and patient satisfaction.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02440542
Study type Observational
Source University of Tennessee
Contact
Status Withdrawn
Phase
Start date May 2015
Completion date May 2018
View Details
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