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
- Diseases
- Alzheimer disease
- 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
Sites (31)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU d'Amiens Centre Mémoire Ressources Recherche Coordinator of this site? Confirm its status | Amiens | France | Unknown status |
| CHU d'Angers Centre Mémoire Ressources Recherche Coordinator of this site? Confirm its status | Angers | France | Unknown status |
| CHU de Bastia Centre Mémoire Ressources Recherche Coordinator of this site? Confirm its status | Bastia | France | Unknown status |
| CHU de Besançon Centre Mémoire Ressources Recherche Coordinator of this site? Confirm its status | Besançon | France | Unknown status |
| CHU de Bordeaux - Service de Neurologie - Centre Mémoire Ressources Recherche - Coordinator of this site? Confirm its status | Bordeaux | France | Unknown status |
| CHRU Cavale Blanche Service de Gériatrie Coordinator of this site? Confirm its status | Brest | France | Unknown status |
| Service de Neuropsychologie Hôpital Neurologique Pierre Wertheimer Coordinator of this site? Confirm its status | Bron | France | Unknown status |
| CHU Côte de Nacre Service de neurologie et CMRR Coordinator of this site? Confirm its status | Caen | France | Unknown status |
| CHU de Clermont Ferrand Centre Mémoire Ressources Recherche Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| Hôpital Pasteur Service de Neurologie Coordinator of this site? Confirm its status | Colmar | France | Unknown status |
| CHU de Dijon- CMRR Coordinator of this site? Confirm its status | Dijon | France | Unknown status |
| Chu de Grenoble CMRR, Neurologie Coordinator of this site? Confirm its status | Grenoble | France | Unknown status |
| Hôpital Roger Salengro CMRR Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| CHU Limoges Service de neurologie et CMRR Coordinator of this site? Confirm its status | Limoges | France | Unknown status |
| AP-HM Coordinator of this site? Confirm its status | Marseille | France | Unknown status |
| CHU Montpellier Hôpital Gui de Chauliac CMRR Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| CHU de Nantes Clinique Neurologique Hôpital GR Laennec Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
| Institut Claude Pompidou Centre Mémoire de Ressources et de Recherche Coordinator of this site? Confirm its status | Nice | France | Unknown status |
| Hôpital Universitaire de la Pitié Salpêtrière Pavillon François Lhermitte Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP Hôpital Broca Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| APHP Groupe Hospitalier Saint Louis Lariboisière Fernand Widal CMRR Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| CHU La Milétrie Pôle de Gériatrie Coordinator of this site? Confirm its status | Poitiers | France | Unknown status |
| CHU Reims Hôpital Maison Blanche Court Séjour Gériatrique Coordinator of this site? Confirm its status | Reims | France | Unknown status |
| CHU de Rennes - Hôpital Pontchaillou / Service de Neurologie Coordinator of this site? Confirm its status | Rennes | France | Unknown status |
| CHU de Rouen Hôpital Charles Nicolle Service Neurologie Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
| Chu de Saint-Etienne, CMRR Coordinator of this site? Confirm its status | Saint-Etienne | France | Unknown status |
| Chu de Strasbourg Hôpital Ka Robertsau Pôle de Gériatrie - CMRR Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
| Centre de Recherche Clinique du Gérontopôle Cité de la Santé Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| CHRU de Bretonneau Unité de gérontopsychiatrie Coordinator of this site? Confirm its status | Tours | France | Unknown status |
| CHU Nancy Service de Gériatrie-CMRR Coordinator of this site? Confirm its status | Vandœuvre-lès-Nancy | France | Unknown status |
| Hospice Civil de Lyon Hôpital des Charpennes Coordinator of this site? Confirm its status | Villeurbanne | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.