MedPath

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

Not Applicable
Completed
Conditions
Parkinson Disease
Registration Number
NCT02907723
Lead Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
5
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
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
mean sleep duration per night15 days
mean sleep onset latency15 days
mean number of awakenings per night15 days
Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.