Radial, Sequential Compression Device Deep Venous Thrombosis Detection Study
Withdrawn before enrolling · Not applicable
Conditions studied: Deep Venous Thrombosis
In brief
The purpose of this study is to evaluate the effectiveness of a new leg compression device in preventing post-surgical deep vein thrombosis (blood clot) that can occur after major and complex spine surgery. The investigators aim to show that this new compression device is no worse than the standard sequential compression device (SCD) at preventing DVT and may be able to detect deep vein thrombosis in patients who are not typically screened for this diagnosis after surgery. This new device may be able to capture an important post-surgical complication while providing a more comfortable treatment option.
Key facts
- Study ID
- NCT04232501
- Run by
- Stanford University
- People needed
- 0
- Starts
- 2021-01-08
- Expected to finish
- 2021-01-08
- Last updated by the study team
- 2021-01-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients scheduled for complex spine surgery at Stanford Hospital
You may not qualify if…
- Pregnancy
- Non-decisional capacity
- Incarcerated persons
- Any hereditary or acquired coagulopathy
Where it is running
- Stanford Hospital and Clinics — Stanford, California, United States
Full record on ClinicalTrials.gov
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