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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03818971
Other study ID # RIPH 2018-02
Secondary ID IDRCB 2018-A0233
Status Completed
Phase N/A
First received
Last updated
Start date May 13, 2019
Est. completion date March 22, 2021

Study information

Verified date October 2021
Source Centre Psychothérapique de Nancy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Alcohol is a major public health problem and its neurotoxic effects are, among other things, responsible for altering the functioning of cerebral neurotransmission pathways. The retina is an anatomical and developmental extension of the central nervous system. It is composed of several layers of retinal neurons that share similar anatomical and functional properties with brain neurons. Retinal neurons are notably equipped with a complex system of neurotransmission constituted by the main neurotransmitters that are involved in the central effects of alcohol: glutamate, dopamine, serotonin ... The retina is used here as a site of indirect investigation for abnormal central neurotransmission pathways following regular alcohol use. It is recognized to date as a good site for investigating central abnormalities in neuropsychiatric and addictive disorders. The objective of this project is to study the retinal function using electroretinogram (ERG) in regular alcohol users to isolate potential markers of cerebral neurotransmission abnormalities.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date March 22, 2021
Est. primary completion date March 22, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility For alcohol consumer with alcohol use disorder : Inclusion Criteria: - aged between 18 and 35 years - alcohol use disorder according to the DSM 5 - affiliation to a social security scheme Exclusion Criteria: - psychoactive substance consumption (other than alcohol) - psychiatric disease in progress according to the DSM 5 - neurologic disease in progress - mental impairment making it difficult or impossible to participate to the study - major under guardianship or curatorship or under safeguarding of justice - pregnant women or feeding - people in emergency situation - participation to another interventional study - retinal disease in progress - chronic glaucoma - ophtalmic disease affecting the visual acuity - ocular infection in progress - urinary positive drug check the day of the inclusion - postive Breathalyser the day of the inclusion

Study Design


Related Conditions & MeSH terms


Intervention

Other:
electroretinogram (flash, pattern and multifocal)
we measured the waves a, b, oscillatory potentials, back ground noise and i for the flash ERG, the waves P50 and N95 for the pattern ERG and the P1, N1 and N2 for the multifocal ERG

Locations

Country Name City State
France Centre Psychothérapique de Nancy Laxou Nancy

Sponsors (1)

Lead Sponsor Collaborator
Centre Psychothérapique de Nancy

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary modification of amplitude measured with flash electroretinogram and pattern electroretinogram / amplitude in microvolt Day 0 (=day of inclusion = the only visit of the study)
Primary modification of implicite time parameters measured with flash electroretinogram and pattern electroretinogram - implicite time in millisecond Day 0 (=day of inclusion = the only visit of the study)
Primary modification of amplitude of the oscillatory potential waves P1, P2, P3, P4 measured with flash electroretinogram - amplitude in microvolt Day 0 (=day of inclusion = the only visit of the study)
Primary modification of implicit time of the oscillatory potential waves P1, P2, P3, P4 measured with flash electroretinogram - implicite time in millisecond Day 0 (=day of inclusion = the only visit of the study)
Primary modification of amplitude of the background noise measured with the flash electroretinogram, flicker 3.0 sequence - amplitude in microvolt Day 0 (=day of inclusion = the only visit of the study)
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