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Completed

NCT Number: NCT01662427

Nocturnal Parkinson's Disease Symptoms Study Group

To study associate factor of Noctural Parkinson's Disease Symptoms and quality of life in Parkinson's disease patients and caregivers.

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Key information

Age range

30 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Roongroj Bhidayasiri

Pathumwan, Bangkok, 10330, Thailand

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Idiopathic Parkinson's disease patient

Exclusion criteria

  • Patient with Secondary Parkinsonism eg.Drug-induced Parkinsonism, Vascular Parkinsonism, exposure to toxin, Encephalitis
  • Patient with Atypical Parkinsonial Syndromes eg. Parkinson-plus syndrome, Progressive Supranuclear Palsy (PSP), Corticobasal Degeneration (CBD)
  • Patient with Heredodegenerative parkinsonism eg. Spinocerebellar ataxias, Wilson's disease, Juvenile Huntington's disease

Treatment and study plan

Questionaire to assess Noctural Parkinson's Disease Symptoms

Other

Questionaire to assess Noctural Parkinson's Disease Symptoms and quality of life

Primary outcomes

  1. To assess Noctural Parkinson's Disease Symptoms

Secondary outcomes

  1. To assess quality of life in Parkinson's Disease patient

  2. To assess quality of life in caregiver of Parkinson's Disease patient

Sponsors and collaborators

Lead sponsor

Chulalongkorn University

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Aug 10, 2012
Registry last updated
Aug 20, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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