Restless Legs Syndrome Clinical Trial
Official title:
Non Interventional Observational Study to Collect Data for the Effect of Switching to Neupro® on Severity of Restless Leg Syndrome (RLS) Symptoms and Augmentation as Well as the Change in Treatment Regimen Used, in RLS Patients With Previous Augmentation
The objective is to assess the effect of Neupro® on the severity of Restless Leg Syndrome (RLS) symptoms and augmentation in patients with augmentation associated with previous oral dopaminergic therapy. In addition, the change in treatment regimen used when switching to Neupro® will be evaluated.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
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Phase 4 | |
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Phase 3 | |
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Phase 1/Phase 2 | |
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||
| Completed |
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|
N/A | |
| Not yet recruiting |
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Phase 4 | |
| Recruiting |
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| Withdrawn |
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| Completed |
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