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

NCT02440542 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2018-11-29

No results posted yet for this study

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.

Conditions

  • Pain, Postoperative

Interventions

OTHER

Survey of outcomes following popliteal nerve block

Patients will be instructed to complete journals of pain and narcotic use until postoperative day 10. On first follow-up visit, patients will complete a patient satisfaction survey. VAS Pain scores and pain medication use will be collected up to 12 weeks postoperatively.

Sponsors & Collaborators

  • University of Tennessee

    lead OTHER

Principal Investigators

  • Jesse F Doty, MD · University of Tennessee College of Medicine Chattanooga/Erlanger Health System

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2018-05-31
Completion
2018-05-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02440542 on ClinicalTrials.gov