Parkinson Disease Clinical Trial
— BRACELETOfficial title:
Assessment of a Wrist Device Recording Sleep Parameters, Before and After Deep Brain Stimulation for Parkinson's Disease
| Verified date | February 2018 |
| Source | Fondation Ophtalmologique Adolphe de Rothschild |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This pilot study aims to assess a new device designed for an objective measure of sleep parameters. The purpose of the device is to assess, in a more simple and precise way, the impact of deep brain stimulation on patient's sleep.
| Status | Completed |
| Enrollment | 5 |
| Est. completion date | June 2016 |
| Est. primary completion date | June 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - patient > 18 years old - with Parkinson disease - scheduled for implantation of electrodes for deep brain stimulation Exclusion criteria: - pregnant or breast feeding patient - refusal to participate in the study - patient under legal protection - no health insurance coverage |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Fondation Ophtalmologique Adolphe de Rothschild | Teva Pharmaceutical Industries, Ltd. |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | mean sleep duration per night | 15 days | ||
| Primary | mean sleep onset latency | 15 days | ||
| Primary | mean number of awakenings per night | 15 days |
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