UnknownPhase 4

Effect of Slow-release Melatonin (Circadin®) Therapy on Idiopathic RBD: a Pilot Study

South Korea30 participantsStarted 2016-01

Plain-language summary

To evaluate effect of slow-release melatonin (Circadin) on REM sleep behavior disorder.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * REM sleep behavior disorder according to ICSD-3 criteria * No cognitive deficit or symptom of Parkinsonism * Those with written consent. Exclusion Criteria: * who took medication (ex. clonazepam) for REM sleep behavior disorder * with degenerative neurologic disorder (ex. Parkinson's disease, Multiple System Atrophy, Lewy-body dementia, etc.) * who took medication that can affect REM sleep behavior disorder (anti-depressant: SSRI, TCA, MAO-inhibitor) * who is unable to answer questionnaires * who have hypersensitive reaction to medications * Pregnant women or breastfeeding * who are diagnosed with other parasomnia disorder * with severe medical disorder (severe liver failure, respiratory failure, heart failure, malignant tumor, etc.)

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Changes in Clinical Global Impression scale

Timeframe: baseline and 4 weeks

Changes in RBDQ-HK score (RBD questionnaire-HK)

Timeframe: Baseline and 4 weeks

Trial details

NCT IDNCT02836743

SponsorSeoul National University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-12-31

Contact for this trial

Ki-Young Jung, M.D. Ph.D.

+82-2-2072-4988 jungky10@gmail.com

View on ClinicalTrials.gov More REM Sleep Behavior Disorder trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.