AI tool aims to cut risky drug combos in seniors, but trial stalls
NCT ID NCT04710615
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested an artificial intelligence platform called Synapse to help doctors avoid dangerous drug interactions in older patients (65+). The goal was to see if the AI could reduce inappropriate prescriptions when patients left the hospital. However, the trial was terminated early, so we don't have enough data to know if it worked. The study involved 178 older adults in French hospitals.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Synapse platform (AI virtual assistant for medication review)
- What this could lead to
- If successful, this could help doctors prescribe safer medications for older adults by catching harmful drug interactions.
- What could go wrong
- The trial was terminated early, so we don't have clear results. It's unclear if the AI platform actually improves prescribing in real-world hospital settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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178 people
The number who actually took part.
- Started
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Oct 2021
- Finished
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Apr 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* Inclusion criteria: * Male or female age aged more than 65 years * Hospitalization in geriatric department at Bordeaux University Hospital or Libourne Hospital * Initial drug prescription with at least 2 active pharmaceutical ingredients * Affiliation to French social security * Written informed consent signed by participant and investigator * Exclusion criteria: * Adults protected by law * Subject included in a clinical trial with an experimental treatment * Subject during exclusion period relative to another trial
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU de Bordeaux
Bordeaux, 33000, France
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CHU de Bordeaux, Hôpital Pellegrin
Bordeaux, 33000, France
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CHU de Bordeaux, Hôpital Xavier Arnozan
Pessac, 33400, France
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CHU de Bordeaux, Hôpital Xavier Arnozan
Pessac, 33600, France
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Centre Hospitalier de Libourne - Pôle Gériatrie
Libourne, 33500, France
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