New sleep drug aims to help Parkinson's patients get a good Night's rest

NCT ID NCT07714772

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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

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Status unknown
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First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time

Summary

This study tests whether dimdazenil, a sleep medication, can safely improve sleep in people with Parkinson's disease who also have insomnia. Researchers will measure sleep changes using overnight brain-wave recordings. The trial involves 50 adults with mild-to-moderate Parkinson's and poor sleep.

What this could mean

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

Active substance
dimdazenil, a GABAA receptor partial agonist
What this could lead to
If successful, dimdazenil could offer a new treatment option for insomnia in Parkinson's disease, potentially improving sleep quality and overall well-being.
What could go wrong
This is a small, early-stage study with only 50 participants, so results may not apply to everyone. The drug may cause side effects or fail to improve sleep significantly.

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.

Participants

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Dec 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.

Who is studied

Parkinson's disease with insomnia,aged ≥18 years, male or female

Ages

18 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: * Provide written informed consent voluntarily after full comprehension of the study. * Be aged ≥18 years, male or female. * Meet the diagnostic criteria for Parkinson's disease according to the Chinese Diagnostic Criteria for Parkinson's Disease (2016 Edition), with a modified Hoehn-Yahr stage ≤3. * Have insomnia symptoms \[reduced total sleep time (\<6.5 h) and/or sleep-onset latency \>30 min, and/or ≥2 nocturnal awakenings, early-morning awakening, or poor sleep quality\], occurring at least three times per week, accompanied by daytime dysfunction or daytime distress, with adequate opportunity for sleep yet difficulty initiating or maintaining sleep, and that cannot be fully explained by another sleep-wake disorder; and have satisfactory control of Parkinson's disease motor symptoms \[MDS-UPDRS Part III (ON state) score ≤30\]. * Be on a stable anti-Parkinsonian medication regimen, defined as no change in the type, dosage, or frequency of anti-Parkinsonian drugs for at least 4 weeks prior to enrollment, with no motor fluctuations or dyskinesia. * Have a clinical decision by the attending physician to initiate didazinin treatment per routine practice. * Be able to undergo polysomnography (PSG) monitoring. * Be conscious, capable of normal communication, and able to complete sleep diaries independently. Exclusion Criteria: * Have Parkinson-plus syndromes, secondary parkinsonism, or other non-idiopathic Parkinson's disease. * Have used benzodiazepine sedative-hypnotics within 7 days prior to enrollment. * Have other significant comorbidities, such as malignant tumors, or clinically significant impairment of cardiac, hepatic, or renal function. * Have severe obstructive sleep apnea (OSA), chronic obstructive pulmonary disease (COPD), respiratory insufficiency, or myasthenia gravis. * Have known hypersensitivity to any component of didazinin. * Have moderate-to-severe depression or anxiety, defined as a Hamilton Depression Rating Scale (HAMD) score ≥25 or a Hamilton Anxiety Rating Scale (HAMA) score ≥29. * Have a history of substance abuse (e.g., drug addiction or alcohol dependence). * Have a history of epilepsy, schizophrenia, bipolar disorder, developmental delay, or cognitive impairment. * Be pregnant or breastfeeding. * Be unwilling or unable to comply with scheduled follow-up visits. * Have any other condition that, in the investigator's judgment, would make the subject unsuitable for participation (e.g., anticipated inability to complete follow-up within 14 days, or concurrent use of other medications that may substantially interfere with sleep assessment and cannot be withdrawn).

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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.

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