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Trial of Valproic Acid in Patients With Progressive Supranuclear Palsy (Depakine)

Primary Purpose

Progressive Supranuclear Palsy

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
valproic acid
Placebo
Sponsored by
Nantes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Progressive Supranuclear Palsy focused on measuring Progressive supranuclear palsy (PSP)

Eligibility Criteria

45 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with possible or probable PSP
  • from 45 to 75 year of age

Sites / Locations

  • Service de Neurologie A, Hôpital Gabriel Montpied-BP
  • Service de Neurologie et Pathologie du mouvement Hôpital Roger Salingro, CHRU de Lille
  • Service de Neurologie, CHU Nantes
  • Service de Neurologie, CHU Poitiers

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

valproic acid

Placebo

Arm Description

Depakine

Placebo

Outcomes

Primary Outcome Measures

PSPRS score (specific score for PSP)

Secondary Outcome Measures

Neuropsychological evaluation

Full Information

First Posted
October 10, 2006
Last Updated
November 2, 2012
Sponsor
Nantes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00385710
Brief Title
Trial of Valproic Acid in Patients With Progressive Supranuclear Palsy (Depakine)
Official Title
Randomized Placebo-controlled Trial of Valproic Acid in Patients With Progressive Supranuclear Palsy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2011
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nantes University Hospital

4. Oversight

5. Study Description

Brief Summary
Progressive Supranuclear Palsy (PSP) is a relentlessly progressive neurodegenerative disorder, clinically characterized by parkinsonism with prominent axial involvement and postural instability, bulbar symptoms, supranuclear ophthalmoplegia, and executive dysfunction. Abnormal neuronal and glial tau aggregations affecting the basal ganglia and selective brainstem structures result in dysfunction of the five frontosubcortical circuits and brainstem functions. There is no effective treatment for PSP. One of the key feature in the aggregation of tau is its phosphorylation by kinases such as glycogen synthase kinase 3b (GSK3b). Recent reports have shown that valproic acid was able to inhibit the activity of GSK3b and could exert a neuroprotective effect through this inhibition. The investigators thus decided to conduct this controlled study to assess the putative neuroprotective effects in patients with PSP.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Progressive Supranuclear Palsy
Keywords
Progressive supranuclear palsy (PSP)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
valproic acid
Arm Type
Experimental
Arm Description
Depakine
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
valproic acid
Intervention Description
Depakine
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
PSPRS score (specific score for PSP)
Time Frame
This score will be measured every three months during the two-year follow up of the study
Secondary Outcome Measure Information:
Title
Neuropsychological evaluation
Time Frame
inclusion, one year and two years follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with possible or probable PSP from 45 to 75 year of age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pascal Derkinderen
Organizational Affiliation
Nantes University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service de Neurologie A, Hôpital Gabriel Montpied-BP
City
Clermont-Ferrand
ZIP/Postal Code
63009
Country
France
Facility Name
Service de Neurologie et Pathologie du mouvement Hôpital Roger Salingro, CHRU de Lille
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
Service de Neurologie, CHU Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
Service de Neurologie, CHU Poitiers
City
Poitiers
ZIP/Postal Code
86021
Country
France

12. IPD Sharing Statement

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Trial of Valproic Acid in Patients With Progressive Supranuclear Palsy (Depakine)

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