Can a sleep drug slow memory decline?
NCT ID NCT05209035
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether the sleep medication trazodone can slow memory loss in people with mild cognitive impairment and obstructive sleep apnea. Researchers will measure changes in blood markers and thinking skills over one year. 134 participants are enrolled in this double-blind, placebo-controlled trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Trazodone
- What this could lead to
- If it works, this could point toward a treatment that slows memory loss in people with mild cognitive impairment and sleep apnea.
- What could go wrong
- This is a small, early-phase trial testing a biomarker, not a proven treatment. The drug may not slow cognitive decline, and side effects like drowsiness are possible.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 134 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
May 2022
- Expected to finish
-
Feb 2026
An estimate. End dates often move.
- Lead sponsor
-
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
-
60 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * Able to swallow trazodone capsules * Stable pharmacological treatment of any other chronic conditions for at least 30 days prior to screening * A diagnosis of mild cognitive impairment (MCI) * A diagnosis of obstructive sleep apnea (OSA), and Apnea-Hypopnea Index \> 5 * Neuroimaging obtained during screening consistent with a clinical diagnosis of Alzheimer's disease (AD) and without findings of significant exclusionary abnormalities * Written informed consent to participate in the study provided by the patient Exclusion Criteria: * Diagnosis of dementia, neurodegenerative condition, seizure disorder or other infectious, metabolic, or systemic disease affecting the central nervous system * Vitamin B12 or folate deficiency * Diagnosis of mental health disorders * Nootropic drugs except for AD prescriptions stable for at least 30 days * Suspected or known allergy to trazodone * Intake of drugs or substances potentially involved in clinically significant inhibition or induction of CYP34A or P-gp-medicate drug interactions with trazodone within 4 weeks or 5 half-lives of the interacting drug prior to administration of trazodone and throughout the course of the study * Previous exposure to anti-Aβ vaccines * Concurrent treatment with antipsychotic agents, antiepileptics centrally active antihypertensive drugs, sedatives, opioids, mood stabilizers, or benzodiazepines within 4 weeks of screening visit * Patients who are receiving non-benzodiazepine hypnotics * Clinically significant, advanced, or unstable disease that might interfere with outcome evaluations
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The Chinese University of Hong Kong
Hong Kong, Hong Kong
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Other studies related to the condition(s) this trial covers.
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