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NOT YET RECRUITING
NCT03454646
PHASE4

Comparison of Therapeutic Strategies With Cholinesterase Inhibitors (SOS TRIAL)

Sponsor: University Hospital, Bordeaux

View on ClinicalTrials.gov

Summary

Cholinesterase inhibitors (CI) remain the only drugs with a recognized efficacy in mild to moderate Alzheimer's disease (AD) in spite of enormous research efforts. However, these drugs presented as "symptomatic treatment" of AD are considered as having only a weak effect on the course of AD. The reimbursement of these drugs is regularly challenged due to the lack of evidence for the impact of these drugs on milestones stages of AD evolution (survival without severe dementia, restriction in Basic Activities of Daily Living - BADL) and on major consequences in public health (hospitalization and institutionalization). The great majority of previous randomized controlled trials conducted with CI have had a too short duration and the end points were limited to cognition (ADAS Cog scale), IADL (Instrumental Activities of Daily Living) function and Global Impression of Change. New evidences from the DOMINO trial (1) conducted in UK, independently of the pharmaceutical industry, showed that the true effect of CI might be more to avoid or to delay the cognitive or functional decline in AD than to improve patients; the institutionalisation (2) was also delayed. However, this trial was conducted in patients with moderate to severe AD, and the interest of the drugs at the mild to moderate stage remains questionable. The investigators have shown that a good surrogate marker of survival without severe dementia would be an increase of ADAS Cog scale of more than six points (3). A post hoc reanalysis of the pivotal RCT with two CI showed that in mild to moderate patients, CI was associated with a 15% decrease of patients with a deterioration of ADAS-Cog of more than six points in six months. Thus at the beginning of dementia the real effect of CI might be more of delaying the cognitive and functional decline, than to improve the patients. The main objective of the SOS trial is to demonstrate that the benefit of CI at the early phase of dementia is the same as at the later phase.

Official title: Comparison of Therapeutic Strategies With Cholinesterase Inhibitors: Stop or Still (SOS) Trial

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

INTERVENTIONAL

Enrollment

1205

Start Date

2024-06-01

Completion Date

2027-09-15

Last Updated

2023-10-06

Healthy Volunteers

No

Interventions

DRUG

cholinesterase inhibitors (CI) (donepezil, galantamine or rivastigmine)

The choice of the treatment will be done by the specialist according to his habits; the specialist will monitor the treatment as usual. All the recruited patients will be treated by CI according to the recommendations of the French HAS and the clinician's habits to choose the type of CI and adjust the dosage. After a 6-month period under CI treatment, patients will be classified according to the evolution of the Mini Mental State Examination (MMSE) as "non-responders" or responders. Responders patients will continue their treatment according to the habits of the clinician. Non-responder patients will be included in the RCT, with individual randomization in two groups: one group who stops the CI, one group who continues the CI. All randomized patients will then be followed-up for two years with regular assessment of judgment criteria every 6 months.

Locations (31)

CHU d'Amiens Centre Mémoire Ressources Recherche

Amiens, France

CHU d'Angers Centre Mémoire Ressources Recherche

Angers, France

CHU de Bastia Centre Mémoire Ressources Recherche

Bastia, France

CHU de Besançon Centre Mémoire Ressources Recherche

Besançon, France

CHU de Bordeaux - Service de Neurologie - Centre Mémoire Ressources Recherche -

Bordeaux, France

CHRU Cavale Blanche Service de Gériatrie

Brest, France

Service de Neuropsychologie Hôpital Neurologique Pierre Wertheimer

Bron, France

CHU Côte de Nacre Service de neurologie et CMRR

Caen, France

CHU de Clermont Ferrand Centre Mémoire Ressources Recherche

Clermont-Ferrand, France

Hôpital Pasteur Service de Neurologie

Colmar, France

CHU de Dijon- CMRR

Dijon, France

Chu de Grenoble CMRR, Neurologie

Grenoble, France

Hôpital Roger Salengro CMRR

Lille, France

CHU Limoges Service de neurologie et CMRR

Limoges, France

AP-HM

Marseille, France

CHU Montpellier Hôpital Gui de Chauliac CMRR

Montpellier, France

CHU de Nantes Clinique Neurologique Hôpital GR Laennec

Nantes, France

Institut Claude Pompidou Centre Mémoire de Ressources et de Recherche

Nice, France

APHP Hôpital Broca

Paris, France

Hôpital Universitaire de la Pitié Salpêtrière Pavillon François Lhermitte

Paris, France

APHP Groupe Hospitalier Saint Louis Lariboisière Fernand Widal CMRR

Paris, France

CHU La Milétrie Pôle de Gériatrie

Poitiers, France

CHU Reims Hôpital Maison Blanche Court Séjour Gériatrique

Reims, France

CHU de Rennes - Hôpital Pontchaillou / Service de Neurologie

Rennes, France

CHU de Rouen Hôpital Charles Nicolle Service Neurologie

Rouen, France

Chu de Saint-Etienne, CMRR

Saint-Etienne, France

Chu de Strasbourg Hôpital Ka Robertsau Pôle de Gériatrie - CMRR

Strasbourg, France

Centre de Recherche Clinique du Gérontopôle Cité de la Santé

Toulouse, France

CHRU de Bretonneau Unité de gérontopsychiatrie

Tours, France

CHU Nancy Service de Gériatrie-CMRR

Vandœuvre-lès-Nancy, France

Hospice Civil de Lyon Hôpital des Charpennes

Villeurbanne, France