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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02704195
Other study ID # 2013-A01323-42
Secondary ID
Status Terminated
Phase N/A
First received March 4, 2016
Last updated September 20, 2016
Start date April 2014
Est. completion date April 2016

Study information

Verified date September 2016
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Interventional

Clinical Trial Summary

Impact of unilateral modulation of deep brain stimulation of the subthalamic nucleus on freezing of gait in Parkinson's disease


Description:

Unilateral modulation of subthalamic stimulation and its impact on freezing of gait in Parkinson's disease will be studied.

In a cross-over, doubleblind, randomized study, a 30% reduction of stimulation intensity of the less impacted side will be compared with chronic treatment with regard to frequency and duration of freezing of gait episodes.


Recruitment information / eligibility

Status Terminated
Enrollment 12
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

Patients affiliated to social security Patient with idiopathic parkinson's disease, with deep brain stimulation since at least one year Freezing of gait Able to give inform consent

Exclusion Criteria:

Patient under guardianship, legal guardianship Psychosis Severe depression Severe cognitive troubles (Mattis < 130) Other neurologic or medical pathology interfering with gait

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Unilateral reduction of stimulation
30% unilateral reduction of Subthalamic nucleus stimulation
Chronic Subthalamic nucleus stimulation
This arm is the reference, with the best stimulation parameters

Locations

Country Name City State
France CHU Grenoble Grenoble

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary improvement of Freezing of gait the improvement will be measure with a composite score of items 12 + 13 on UPDRS II and items 10+11 on UPDRS III, 1 month after new stimulation parameters Yes
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