Suspended
PETHOXICOEvaluation of the Threshold for the Interpretation of the Results of a Method for the Blood Determination of Phosphatidyléthanol
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Alcoholism+2
+ Mental Disorders
+ Substance-Related Disorders
Over 18 Years
+5 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: September 2021
Summary
Principal SponsorUniversity Hospital, Lille
Study ContactOlivier COTTENCIN, MD,PhD
Last updated: January 28, 2026Sourced from a government-validated database.Claim as a partner
Study start date: September 1, 2021
Actual date on which the first participant was enrolled.For an analytical validation of the method for the determination of blood hosphatidylethathanol, it is necessary to: * to compare the results of chronic and excessive ethanol patients with the cut-off proposed in the literature. * Also assess the stability of phosphatidylethanol in total blood collected, and in blotted dried blood stains (DBS), depending on temperature (ambient temperature and +4°C)
Official TitleEvaluation of the Threshold for the Interpretation of the Results of a Method for the Blood Determination of Phosphatidyléthanol
Principal SponsorUniversity Hospital, Lille
Study ContactOlivier COTTENCIN, MD,PhD
Last updated: January 28, 2026Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
AlcoholismMental DisordersSubstance-Related DisordersAlcohol-Related DisordersChemically-Induced Disorders
Criteria
2 inclusion criteria required to participate
Person with alcohol consumption ≥ 40g/day (women) and ≥ 60g/day (men) according to WHO criteria
Person hospitalized for a hospital withdrawal in the addiction service of Lille's hospital, without other distinctions.
3 exclusion criteria prevent from participating
Patient opposing the use of their personal data in the study
Patient subject to protective measures (guardianship or curatorship)
Person deprived of liberty
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has no location dataSave this study to your profile to know when the location data is available.
SuspendedNo study centers