Effect of Melatonin on Sleep Disturbances in Patients With Parkinson's Disease
Launched by KUHNIL PHARMACEUTICAL CO., LTD. · May 9, 2016
Trial Information
Current as of June 19, 2025
Unknown status
Keywords
ClinConnect Summary
After selecting patients who satisfied the inclusion criteria and were not disqualified by the exclusion criteria, through a double-blind procedure the patients are directed to orally take either the investigational drug melatonin or a placebo(allocation ratio 1:1) for 4 weeks, once daily, before going to sleep. The evaluation of efficacy and safety is performed at the first baseline and immediately after administering the drug for 4 weeks.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients who meet the clinical criteria for idiopathic Parkinson's disease (United Kingdom Parkinson's Disease Brain Bank Criteria)
- • 2. Patients who complain of sleep disturbances such as insomnia, REM sleep behavior disorder, excessive daytime sleepiness (EDS), etc.
- • 3. Patients who have received drug treatment for at least 6 months since their diagnosis
- • 4. Male or female patient aged 55 or older
- • 5. Patients who have given voluntary consent after understanding the content of the clinical trial (in the case of elderly patients aged 70 or older, consent must be received from both the subject and the his or her legal representative)
- Exclusion Criteria:
- • 1. Patients with a serious cognitive disorder, behavioral disorder, or mental illness
- • 2. Patients with a serious medical disease
- • Patients who concomitantly suffer from severe renal impairment, convulsions, stomach ulcers, moderate or more severe liver disease
- • Patients with un-controlled high blood pressure or diabetes
- • 3. Patients who have taken another drug under clinical trial within 4 weeks prior to registering for this clinical trial, or patients who are pregnant or breastfeeding
- • 4. Patients who have a history of hypersensitivity to the investigational drug or a drug similar in component or who have had heavy metal poisoning
- • 5. Patients who are taking drugs which could effect on sleep such as rivotril, quetiapine, lexapro, etc.
About Kuhnil Pharmaceutical Co., Ltd.
Kuhnil Pharmaceutical Co., Ltd. is a leading pharmaceutical company dedicated to advancing healthcare through innovative drug development and high-quality therapeutic solutions. With a strong commitment to research and development, Kuhnil focuses on creating safe and effective medications across various therapeutic areas, aiming to improve patient outcomes and quality of life. The company adheres to stringent regulatory standards and ethical practices, ensuring the integrity of its clinical trials and fostering collaboration with healthcare professionals and regulatory authorities. Through its efforts, Kuhnil strives to contribute significantly to the global healthcare landscape.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Jisun Kim
Principal Investigator
Soon Chun Hyang University Hospital, Department of Neurology
Jin Whan Cho
Principal Investigator
Samsung Medical Center, Department of Neurology
Eungseok Oh
Principal Investigator
Chungnam National University Hospital, Department of Neurology
Wooyoung Jang
Principal Investigator
Gangneung Asan Hospital, Department of Neurology
Jinse Park
Principal Investigator
Inje University Haeundae Paik Hospital, Department of Neurology
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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