CompletedNot Applicable

Feasibility of Continuous Sleep Recording in Patients Undergoing Deep Brain Stimulation for Parkinson's Disease

5 participantsStarted 2014-12

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

mean sleep duration per night

Timeframe: 15 days

mean sleep onset latency

Timeframe: 15 days

mean number of awakenings per night

Timeframe: 15 days

Trial details

NCT IDNCT02907723

SponsorFondation Ophtalmologique Adolphe de Rothschild

Sponsor typeNETWORK

Study typeINTERVENTIONAL

Primary completion2016-06

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