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Search / Trial NCT02768077

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

Melatonin Sleep Disturbances

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.

Locations

Patients applied

0 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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