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Study of the Distractibility Syndrome in Patients With Progressive Supranuclear Palsy

Study of the Distractibility Syndrome in Patients With Progressive Supranuclear Palsy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00139373
Enrollment
16
Registered
2005-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2007-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Supranuclear Palsy, Progressive

Keywords

Progressive supranuclear palsy, Frontal lobe, Oculomotor testing, Neuropsychological scores, Motor disability (UPDRS), Distractibility

Brief summary

The syndrome of distractibility is a behavioral disorder induced by a lesion or a dysfunction of the frontal lobe. This sign is frequent in patients with progressive supranuclear palsy (PSP), a neurodegenerative disorder with severe neuronal loss in the prefrontal cortex and cholinergic systems, in particular in the Meynert basalis nucleus. This could participate in the occurrence of the distractibility in these patients. The aim of this study is to evaluate the effect of the donepezil, an anticholinesterase, on the distractibility in PSP patients, by using oculomotor and neuropsychological assessments.

Interventions

DRUGdonepezil

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Groupe Hospitalier Pitie-Salpetriere
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with PSP * Age \> 30 years old * Disease duration \< 5 years * Mini mental state (MMS) \> 24 * Antisaccades %: 40-80%

Exclusion criteria

* Other parkinsonian syndromes * MMS \< 24

Countries

France

Contacts

Primary ContactBertrand Gaymard, MD, PhD
gaymard@ccr.jussieu.fr33-142162218
Backup ContactSophie Rivaud-Pechoux, PhD
rivaud@ccr.jussieu.fr33-142162218

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026