The Efficacy of Aldehyde Dehydrogenase Enzyme in Essential Tremor Patients: A Single-Center Study
NCT ID: NCT07124507
Last Updated: 2025-08-15
Study Results
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Basic Information
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ENROLLING_BY_INVITATION
NA
40 participants
INTERVENTIONAL
2025-03-10
2026-02-28
Brief Summary
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Detailed Description
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This single-center, open-label, sponsor-initiated study is funded by PICO Entech Corp and conducted at Korea University Anam Hospital under the supervision of the institutional IRB. The trial aims to evaluate the efficacy and safety of an ALDH-containing food supplement (PICOZYME ET) in patients with ET. A total of 40 adult participants diagnosed with ET will be enrolled and instructed to consume the investigational food product twice daily for three months. Efficacy will be measured by changes from baseline in the Clinical Rating Scale for Tremor (CRST) and Activities of Daily Living (ADL) scores.
Secondary outcomes include safety and biomarker analysis through blood tests. Exploratory outcomes include changes in metabolic activity via FDG PET-CT imaging, levels of oxidative stress biomarkers (malondialdehyde, total aldehyde), and potential associations with GABA-related metabolic pathways.
The study has received IRB approval from Korea University Anam Hospital and includes oversight from a Data Safety Monitoring Board (DSMB). All participants will provide written informed consent before enrollment.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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ALDH Food Supplement
Participants in this arm will receive an ALDH-containing food supplement (PICOZYME ET) twice daily for 3 months. The study will assess changes in tremor severity, quality of life, and exploratory metabolic biomarkers.
PICOZYME ET
The investigational product is a dietary supplement containing aldehyde dehydrogenase (ALDH), administered orally twice daily (one packet in the morning and one in the evening) for 3 months before meals.
Interventions
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PICOZYME ET
The investigational product is a dietary supplement containing aldehyde dehydrogenase (ALDH), administered orally twice daily (one packet in the morning and one in the evening) for 3 months before meals.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Diagnosed with Essential Tremor (ET) by a board-certified neurologist or neurosurgeon.
* Presence of postural or intention tremor in the dominant hand/arm with a CRST score ≥ 2.
* Stable medication regimen for at least 30 days prior to enrollment.
* No structural brain abnormalities on MRI within the last 3 years.
* Eligible according to investigator assessment and agreement by two clinical team members.
Exclusion Criteria
* Significant medical conditions such as severe arrhythmia, renal failure, hepatic failure, acute stroke, or epilepsy.
* Contraindications to MRI (e.g., pacemakers, metal implants).
18 Years
ALL
No
Sponsors
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Korea University Anam Hospital
OTHER
Responsible Party
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Locations
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Korea University Anam Hospital
Seoul, , South Korea
Countries
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References
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Louis ED, Ferreira JJ. How common is the most common adult movement disorder? Update on the worldwide prevalence of essential tremor. Mov Disord. 2010 Apr 15;25(5):534-41. doi: 10.1002/mds.22838.
Related Links
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Related Info
Other Identifiers
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2024AN0506
Identifier Type: -
Identifier Source: org_study_id
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