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Could an antidepressant shield the brain in Parkinson's?

NCT ID NCT04497168

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether taking citalopram for 26 months could slow the buildup of harmful amyloid plaques in the brain area responsible for visual thinking in people with Parkinson's disease. Fifty-eight participants aged 65 and older were randomly assigned to receive either citalopram or a placebo. The goal was to see if the drug could protect against cognitive decline related to vision and spatial awareness.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
citalopram
What this could lead to
If it works, this could point toward a way to protect thinking skills in Parkinson's disease by reducing harmful brain plaques.
What could go wrong
This is a small, early-phase trial with only 58 participants. The drug may not change plaque levels or thinking, and citalopram can have side effects like nausea or drowsiness.

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 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

58 people

The number who actually took part.

Started

Apr 2021

Finished

Mar 2026

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

65 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Subjects with a Parkinson Disease (PD) diagnosis based on the United Kingdom Parkinson's Disease Society Brain Bank Research Center clinical diagnostic criteria * Modified Hoehn and Yahr (HY) scores spanning 2.0 to 3.0 * Age 65 years or greater Exclusion Criteria: * Diagnosis of an atypical parkinsonian condition * Participants on neuroleptics and participants with a history of use of anti-depressants (including selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), bupropion, St. John's Wort or other serotoninergic agents in the year preceding study enrollment * Evidence of a large artery stroke or mass lesion on brain imaging * Participants with a life threatening comorbid illness * Severe claustrophobia precluding PET imaging * Inability to participate in research procedures involving ionizing radiation * Pregnancy or breastfeeding * Participants with active depression as defined by a Geriatric Depression Scale score of \>10 or on the basis of clinical diagnosis by the PI * Participants who report active suicidal ideation as defined by an affirmative answer to questions 1 and 2 on the C-SSRS * Participants with baseline HY scores \<2.0 or ≥3.0 * Participants with a QTc interval on baseline EKG \>0.45 for men or \>0.47 for women * Subjects taking certain contraindicated medications at baseline * Subjects unable to swallow pills * Subjects with a previous history of mania, ongoing hepatic impairment or epilepsy * Subjects with a known allergy to citalopram or escitalopram * Subjects with substantial cognitive impairment or dementia that would prevent them from providing informed consent * Subjects in another ongoing clinical trial * Subjects with treatment-naieve Parkinson disease

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Conditions

The condition(s) this trial relates to.

Parkinson disease Plaque, Amyloid

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • University of Michigan

    Ann Arbor, Michigan, 48109, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.