Trials / Withdrawn
WithdrawnNCT02440542
Popliteal Nerve Block for Postoperative Pain Control in Ankle and Hindfoot Reconstruction
Popliteal Nerve Block for Postoperative Pain Control in Patients Undergoing Ankle and Hindfoot Reconstruction About the Talus
- Status
- Withdrawn
- Phase
- —
- Study type
- Observational
- Enrollment
- 0 (actual)
- Sponsor
- University of Tennessee · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2015-05-01
- Primary completion
- 2018-05-01
- Completion
- 2018-05-01
- First posted
- 2015-05-12
- Last updated
- 2018-11-29
Source: ClinicalTrials.gov record NCT02440542. Inclusion in this directory is not an endorsement.