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Completed

NCT Number: NCT05638815

An Observational Study of Parkinson's Disease and Other Synucleinopathies (EASE-PD)

The study is a multi-center, observational study to evaluate the feasibility of α-synuclein-related biomarkers and imaging data in the disease diagnosis and prognosis evaluation in Synucleinopathies and healthy subjects.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Union Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei, China

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About this study

In the study, a total number of no more than 100 subjects are planned to be enrolled.

Subjects who are eligible for enrollment will be enrolled in the study after signing the informed consent form (ICF) and undergo 3 visits, including the baseline visit (the day of first blood sample collection), visit 1 (day 183 post-enrollment), and visit 2 (day 366 post-enrollment).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • PD subjects must meet the following criteria to be eligible:
  • Age ≥ 40 years old, regardless of gender;
  • Primary PD is diagnosed according to MDS Clinical Diagnostic Criteria for Parkinson's Disease of the International Movement Disorders Association (MDS) in 2015 and the Diagnostic Criteria of Parkinson's Disease in China in 2016;
  • Hohen & Yahr stage 1-3;
  • Receive standard treatment for at least 4 weeks before the screening visit (standard treatment is listed in the Chinese Guidelines for the Treatment of Parkinson's Disease (Fourth Edition));
  • The subject or his/her legal representative is able to understand the content of the informed consent and provide a signed ICF.
  • MSA subjects must meet the following criteria to be eligible:
  • Age ≥ 40 years old, regardless of gender;
  • Patients with probable and possible MSA are diagnosed according to the Second Consensus Statement on the Diagnosis of Multiple System Atrophy and the Chinese Expert Consensus on the Diagnostic Criteria of Multiple System Atrophy in 2018;
  • The subject or his/her legal representative is able to understand the content of the informed consent and provide a signed ICF.
  • Healthy subjects must meet the following criteria to be eligible:
  • Age ≥ 40 years old, regardless of gender;
  • Volunteers who are in good health for their age as determined by clinical examination at the time of screening and who are free from dyskinesia as determined by a complete neurological assessment and from serious systemic disease as determined by a complete history;
  • Be able to understand the content of informed consent and agree to sign ICF.

Exclusion criteria

  • Excluded if any of the following criteria is met:
  • Secondary Parkinsonism due to infection, vascular, drugs, poisons, trauma and other causes;
  • Malignant neoplasm (except basal or squamous cell skin cancer) diagnosed within the last 5 years;
  • Those with a known mental illness or substance abuse that will cause them to be unable to cooperate;
  • Patients with severe depression or suicidal behavior (including active attempt, interrupted attempt or attempted attempt) or suicidal thoughts in the past 6 months according to the clinical judgment of the investigator;
  • Pregnant or lactating women;
  • Prior treatment with drugs targeting α-synuclein;
  • Received an investigational drug or device within the previous 4 weeks;
  • The results of laboratory examination and serological virological examination are not suitable for enrollment according to the judgment of the investigator;
  • Other conditions judged by the investigator as not suitable for inclusion.

Treatment and study plan

Primary outcomes

  1. To evaluate the difference of α-synuclein-related biomarkers between patients and healthy subjects

    Time frame: 12 months

Secondary outcomes

  1. Attempt to evaluate the correlation between α-synuclein and disease progression by comparing α-synuclein levels at baseline

    Time frame: 6 months, and 12 months

  2. To evaluate the differences of imaging-related indicators in PD, MSA, and their correlation with the disease by brain positron emission tomography (PET)

    Time frame: 12 months

  3. To evaluate the correlation between α-synuclein levels and imaging data.

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

SciNeuro

Industry

Registry information

Official study title

An Observational Study to Explore the Role of Alpha-Synuclein-related Biomarkers in the Diagnosis and Disease Evaluation of Parkinson's Disease and Other Synucleinopathies

Acronym: EASE-PD

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Dec 6, 2022
Registry last updated
Nov 22, 2023

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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