ALS Diagnosis From a Saliva Sample: a Non-coding RNA Analysis Approach

Status: Recruiting
Location: See all (19) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

RNALS is a multicentre, transversal, diagnostic and non-interventional study carried out in ALS reference centers; in order to identify a diagnostic signature for Amyotrophic Lateral Sclerosis by analyzing of coding and non-coding RNA contained in patients saliva. The study population consists of patients with definite or probable amyotrophic lateral sclerosis (ALS) according to the El Escorial criteria (ALS Subjects group) and subjects with no neurological history (Control group). The control group will be made up of caregivers of patients with ALS, and caregivers of patients with a pathology other than ALS. The ALS patients concerned by the study already benefit from routine medical care in ALS expert centers in France. The patients concerned by the study will be managed without modification of the care pathway, nor modification of the therapeutic indications, nor modification of the diagnostic or follow-up examinations necessary according to the context, which are carried out according to the recommendations of the HAS, CNGOF.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Patient over 18 years of age,

• Patient from one of the 2 study populations:

‣ Diagnosis of definite or probable ALS according to El Escorial criteria (patients ALS group) ;

⁃ Control group

• Patient able to carry out a mouth rinse,

• Patient affiliated to the healthcare system,

• Patient has dated and signed the consent form,

Locations
Other Locations
France
CHU Angers
RECRUITING
Angers
CHU Bordeaux
NOT_YET_RECRUITING
Bordeaux
Hôpital Cavale Blanche
RECRUITING
Brest
Hospices Civils de Lyon
RECRUITING
Bron
CHU Caen
RECRUITING
Caen
CHU Clermont-Ferrand
RECRUITING
Clermont-ferrand
CHRU Lille
RECRUITING
Lille
CHU Dupuytren
NOT_YET_RECRUITING
Limoges
Hôpital de La Timone
RECRUITING
Marseille
CHU Montpellier
RECRUITING
Montpellier
CHU Nice
RECRUITING
Nice
Hôpital de la Pitié-Salpêtrière
RECRUITING
Paris
CHU Rennes
RECRUITING
Rennes
C.H.U. de Saint-Étienne
NOT_YET_RECRUITING
Saint-étienne-de-montluc
CHU Nantes
RECRUITING
Saint-herblain
CHU de la Réunion
RECRUITING
Saint-pierre
CHU Strasbourg
NOT_YET_RECRUITING
Strasbourg
CHU Toulouse
RECRUITING
Toulouse
CHU Bretonneau
RECRUITING
Tours
Contact Information
Primary
Philippe Codron, Dr
Philippe.codron@chu-angers.fr
+33 2 41 35 79 33
Time Frame
Start Date: 2023-07-11
Estimated Completion Date: 2025-07
Participants
Target number of participants: 600
Treatments
SLA group
300 patients
Control group
300 patients
Sponsors
Collaborators: Monitoring Force Group
Leads: ZIWIG

This content was sourced from clinicaltrials.gov