Study of Degenerescence CSF Hallmarks in Older Bipolar Patients

NCT ID: NCT02836054

Last Updated: 2019-01-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-11-30

Study Completion Date

2019-12-31

Brief Summary

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Analysis of 4 CSF Alzheimer's disease biomarkers (total and phosphorylated tau protein, Aß40 and Aß1-42) and morphological brain MRI in older patients (\>60 year's old) with bipolar disorder, after an evaluation of their cognitive functions.

Comparison between two groups of patients : patients with cognitive disorders and patients without cognitive disorders.

The objective is to describe and compare the profile of those biomarkers in those two populations.

Detailed Description

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Describe the profile of the 4 neurodegeneration's biomarkers of Alzheimer's disease dosed in the cerebrospinal fluid (Total Tau proteins, phosphorylated, Aß40 and Aß1-42) for old subjects suffering from bipolar disorder with or without cognitive impairment.

Conditions

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Bipolar Disorder Alzheimer's Disease

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Patients with cognitive disorders

lumbar punction + brain MRI

Group Type OTHER

lumbar puncture (LP)

Intervention Type PROCEDURE

brain MRI

Intervention Type PROCEDURE

Patients without cognitive disorders

lumbar punction + brain MRI

Group Type OTHER

lumbar puncture (LP)

Intervention Type PROCEDURE

brain MRI

Intervention Type PROCEDURE

Interventions

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lumbar puncture (LP)

Intervention Type PROCEDURE

brain MRI

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* male or female between 60 and 80
* french-speaking, reading and writing patient
* affiliation to the French Social Security
* written informed consent obtained from the patient
* agree to undergo a lumbar puncture
* easy accessibility for the lumbar puncture
* Mini Mental State Examination (MMSE) \> 20
* bipolar patients :

* type I or II
* state of euthymia for at least 4 weeks
* stable psychotropic drug treatment for at least 8 weeks
* no electroconvulsive therapy during the 6 months before inclusion
* distribution in the "with cognitive disorder" or "without cognitive disorder" group is function of the result of the neuropsychological evaluation


* severe visual or auditory disorder
* advanced lumbar osteoarthritis
* history of severe head injury, neurological disorders, diagnosed dementia
* addiction weaned for less than 12 months
* forced hospitalization in psychiatry
* MRI contraindications
* LP contraindications

Exclusion Criteria

\- at least one of the outcome measures can't be performed :

* MRI
* LP : anticoagulation, bad accessibility
Minimum Eligible Age

60 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Lora COHEN

Role: PRINCIPAL_INVESTIGATOR

CMRR, Pavillon de Neurologie, C.H.U. de Grenoble

Locations

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University Hospital, Grenoble

Grenoble, Isère, France

Site Status RECRUITING

Countries

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France

Central Contacts

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Lora COHEN

Role: CONTACT

0476765790/0476769284

References

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Other Identifiers

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2013-A00930-45

Identifier Type: OTHER

Identifier Source: secondary_id

38RC13.408

Identifier Type: -

Identifier Source: org_study_id

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