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Clinical Trials in France / NCT07830680
Starting soon Observational

Physiopathology of Behavioral Addictions and Biomarkers

NCT07830680 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-10-01
Last updated
2026-09-24

Condition(s) studied

Food AddictionSexual Addiction

Investigational drug(s) / intervention(s)

blood sampling →

blood sampling: One blood sample wiil be collected into a 10mL K2EDTA BD Vacutainer® tube

Study summary

The goal of this observational study is to evaluate the expression of miR-10a-5p in the blood in patients with sexual addiction or food addiction. The main question it aims to answer is : To determine whether adults patients with SA or FA exhibit a distinct blood miR-10a-5p expression profile compared with matched healthy controls.

For all participants, one blood sample will be collected.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion criteria For patients with FA: * Male and females ≥ 18 years old * Already in care or newly initiating care * Participating to EVALADD cohort * Current diagnosis of FA * Oral consent provided * Affiliated with French social security system or beneficiary from such system For healthy controls matched to patients with FA: * Male and females ≥ 18 years old * Oral consent provided * Affiliated with French social security system or beneficiary from such system For patients with SA: * Male ≥ 18 years old * Already in care or newly initiating care * Participating to EVALADD cohort * Current diagnosis of SA * Oral consent provided * Affiliated with French social security system or beneficiary from such system For healthy controls matched to patients with SA: * Male ≥ 18 years old * Oral consent provided * Affiliated with French social security system or beneficiary from such system Exclusion Criteria : For patients with FA: * Presence of a current diagnosis of SA * Presence of any current addictive disorder (substance \[except tobacco\] use disorders, gambling disorder, gaming disorder) * Presence of any current instable psychiatric disorder (requiring the initiation or adapation of medication) * Pregnancy or breastfeeding woman * Trusteeship or curatorship * Major cognitive impairment * Not fluent in French For patients with SA: * Presence of a current diagnosis of FA * Presence of any current addictive disorder (substance \[except tobacco\] use disorders, gambling disorder, gaming disorder) * Presence of any current instable psychiatric disorder (requiring the initiation or adapation of medication) * Trusteeship or curatorship * Major cognitive impairment * Not fluent in French For healthy controls: * Without a current diagnosis of FA * Without a current diagnosis of SA * Presence of any current addictive disorder (substance \[except tobacco\] use disorders, gambling disorder, gaming disorder) * Presence of any current instable psychiatric disorder (requiring the initiation or adapation of medication) * Pregnancy or breastfeeding woman * Trusteeship or curatorship * Major cognitive impairment * Not fluent in French

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Nantes University Hospital Nantes France

More Nantes University Hospital trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07830680 on ClinicalTrials.gov ↗ ← All trials in France