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NCT03454646Not yet recruitingPhase 4

Comparison of Therapeutic Strategies With Cholinesterase Inhibitors (SOS TRIAL)

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

Source: ClinicalTrials.gov · Last updated 6 Oct 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
1205 (estimated)
First submitted
9 Feb 2018
Start date
1 Jun 2024
Primary completion date
27 Apr 2027
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT03454646

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 1205
  • From 1 Jun 2024 to the primary completion date, 27 Apr 2027
  • 31 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • CI responder patients for whom the MMSE score remained stable or became higher after 6 months of treatment
  • Patients with complete dependency for bathing and dressing at the randomization visit
  • Patients residing in an institution at the randomization visit

Who the study is looking for

  • New case of AD referring to a CMRR or MC.
  • Diagnosis of probable or possible AD, defined according to the NINCDS-ARDRA criteria
  • Mild to moderate stage, defined by a MMSE score above 15 at the time of pre-inclusion
  • Patients with indication to CI treatment
  • Patients Naïve to CI treatment
  • Patients aged 50 years or more
  • Menopause or effective contraception (for women)
  • Affiliated person or beneficiary of a social security scheme
  • Patients with AD LTI (Long Term Illeness)
  • Patients agree to participate, with free, informed and written consent signed by the patient and his caregiver
    • Non Inclusion Criteria:
  • Patients diagnosed with Lewy bodies disease, fronto-temporal dementia, or dementia from a cause other than Alzheimer Disease
  • More severe stage of the disease, defined by a MMSE equal or below 15 at the time of inclusion
  • Patients with contraindication to CI treatment
  • Patients residing in an institution at the time of pré-inclusion or randomization
  • Patients with a complete dependency for bathing and dressing at the time of pré-inclusion or randomization ( ADL de Katz, score 2/2 for the item "bathing" and/or "dressing")
  • Patients under tutorship or curatorship, patients unable to express consent
  • Patients with unstable severe general disease compromising the follow-up
  • Patients without caregiver
  • Patients included in another pharmacological trial
  • Pregnant or breastfeeding women

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (31)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU d'Amiens Centre Mémoire Ressources Recherche
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AmiensFranceUnknown status
CHU d'Angers Centre Mémoire Ressources Recherche
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AngersFranceUnknown status
CHU de Bastia Centre Mémoire Ressources Recherche
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BastiaFranceUnknown status
CHU de Besançon Centre Mémoire Ressources Recherche
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BesançonFranceUnknown status
CHU de Bordeaux - Service de Neurologie - Centre Mémoire Ressources Recherche -
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BordeauxFranceUnknown status
CHRU Cavale Blanche Service de Gériatrie
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BrestFranceUnknown status
Service de Neuropsychologie Hôpital Neurologique Pierre Wertheimer
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BronFranceUnknown status
CHU Côte de Nacre Service de neurologie et CMRR
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CaenFranceUnknown status
CHU de Clermont Ferrand Centre Mémoire Ressources Recherche
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Clermont-FerrandFranceUnknown status
Hôpital Pasteur Service de Neurologie
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ColmarFranceUnknown status
CHU de Dijon- CMRR
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DijonFranceUnknown status
Chu de Grenoble CMRR, Neurologie
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GrenobleFranceUnknown status
Hôpital Roger Salengro CMRR
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LilleFranceUnknown status
CHU Limoges Service de neurologie et CMRR
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LimogesFranceUnknown status
AP-HM
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MarseilleFranceUnknown status
CHU Montpellier Hôpital Gui de Chauliac CMRR
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MontpellierFranceUnknown status
CHU de Nantes Clinique Neurologique Hôpital GR Laennec
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NantesFranceUnknown status
Institut Claude Pompidou Centre Mémoire de Ressources et de Recherche
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NiceFranceUnknown status
Hôpital Universitaire de la Pitié Salpêtrière Pavillon François Lhermitte
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ParisFranceUnknown status
APHP Hôpital Broca
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ParisFranceUnknown status
APHP Groupe Hospitalier Saint Louis Lariboisière Fernand Widal CMRR
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ParisFranceUnknown status
CHU La Milétrie Pôle de Gériatrie
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PoitiersFranceUnknown status
CHU Reims Hôpital Maison Blanche Court Séjour Gériatrique
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ReimsFranceUnknown status
CHU de Rennes - Hôpital Pontchaillou / Service de Neurologie
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RennesFranceUnknown status
CHU de Rouen Hôpital Charles Nicolle Service Neurologie
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RouenFranceUnknown status
Chu de Saint-Etienne, CMRR
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Saint-EtienneFranceUnknown status
Chu de Strasbourg Hôpital Ka Robertsau Pôle de Gériatrie - CMRR
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StrasbourgFranceUnknown status
Centre de Recherche Clinique du Gérontopôle Cité de la Santé
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ToulouseFranceUnknown status
CHRU de Bretonneau Unité de gérontopsychiatrie
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ToursFranceUnknown status
CHU Nancy Service de Gériatrie-CMRR
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Vandœuvre-lès-NancyFranceUnknown status
Hospice Civil de Lyon Hôpital des Charpennes
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VilleurbanneFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.