Physiopathology of Behavioral Addictions and Biomarkers

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNantes University Hospital

About this trial

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 criteria

This trial accepts healthy volunteers

Qualifiers

Male and females ≥ 18 years old

Already in care or newly initiating care

Participating to EVALADD cohort

Current diagnosis of FA

Disqualifiers

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

Trial population

Patients with food or sexual addiction, compared with age- and sex-matched healthy controls with no current addictive disorder.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • blood sampling

    Biological/Vaccine

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

Treatment groups

28 Participants
are divided into 2 treatment groups
Group A: Patients with addiction1 intervention
Group B: Healthy controls1 intervention

Trial outcomes

Primary outcomes

1

Blood miR-10a-5p expression

The concentration of each miR-enriched fraction will be determined by spectrophotometric between patients with SA or FA and matched healthy controls.

Time frame
3 months

Secondary outcomes

1

Blood additional circulating miRs expression

The concentration of circulating miRs fraction will be determined by spectrophotometric between patients with SA or FA and matched healthy controls.

Time frame
3 months
2

Clinical Characteristics

Association between blood expression levels of circulating miRs and age

Time frame
3 months
3

Clinical Characteristics

Association between blood expression levels of circulating miRs and sex

Time frame
3 months
4

Clinical Characteristics

Association between blood expression levels of circulating miRs and duration of addiction

Time frame
3 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Nantes University Hospital

Lead sponsor

INSERM U1216 Grenoble Institut des Neurosciences

Collaborator

This trial is not recruiting at the moment. You can still explore other options: