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Enrolling by Invitation

NCT Number: NCT07238725

The Efficacy of Aldehyde Dehydrogenase Enzyme in Essential Tremor Patients: A Single-Center Study

This is a sponsor-initiated, single-arm, single-center clinical trial designed to evaluate the efficacy and safety of an ALDH-containing food supplement (PICOZYME ET) in patients with Essential Tremor (ET). Participants will consume the investigational product daily for three months, and clinical outcomes will be assessed using the Clinical Rating Scale for Tremor (CRST) and the Activities of Daily Living (ADL) scale. Additional exploratory analyses will evaluate changes in metabolic biomarkers and brain function via imaging and blood tests.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Korea University Anam Hospital

Seoul, 02841, South Korea

About this study

Essential Tremor (ET) is one of the most common adult movement disorders, characterized by involuntary rhythmic tremors, primarily affecting the hands. Although not life-threatening, ET significantly impacts quality of life and daily functioning. Recent studies suggest that oxidative stress and impaired GABAergic inhibition may be involved in its pathophysiology, and aldehyde dehydrogenase (ALDH) is believed to play a role in mitigating these mechanisms.

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.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adults aged ≥ 19 years who provide written informed consent.
  • 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

  • Presence of secondary tremor causes (e.g., Parkinsonism, dystonia).
  • Significant medical conditions such as severe arrhythmia, renal failure, hepatic failure, acute stroke, or epilepsy.
  • Contraindications to MRI (e.g., pacemakers, metal implants).

Treatment and study plan

PICOZYME ET

Dietary Supplement

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 names: ALDH food supplement

Primary outcomes

  1. Change in Clinical Rating Scale for Tremor (CRST) total score from baseline to 3 months

    Time frame: Baseline and 3 months

    The CRST is a validated clinical tool used to quantify tremor severity. It includes assessments of postural, action, and intention tremor, as well as functional disability. Total scores range from 0 to 160, with higher scores indicating more severe tremor.

  2. Change in Activities of Daily Living (ADL) score from baseline to 3 months

    Time frame: Baseline and 3 months

    ADL will be assessed using the QUEST (Quality of Life in Essential Tremor) questionnaire. Higher scores indicate greater functional impairment.

Secondary outcomes

  1. Change in 24-hour Urinary Catecholamine Levels (epinephrine, norepinephrine, dopamine)

    Time frame: Baseline and 3 months

    Measurement of 24-hour urinary catecholamine levels (epinephrine, norepinephrine, dopamine) in µg/day at baseline and 3 months to evaluate oxidative stress.

  2. Change in Random Urinary Malondialdehyde

    Time frame: Baseline and 3 months

    Semi-quantitative measurement of malondialdehyde in random urine using dipstick analysis (DFI FRC 50SF analyzer and Free RadiCheck test strips), with results reported as relative values.

  3. Change in Serum C-Reactive Protein (CRP) Level

    Time frame: Baseline and 3 months

    Measurement of serum CRP concentration in mg/L at baseline and 3 months.

  4. Incidence of adverse events during the intervention period

    Time frame: Through study completion (up to 3 months)

    Adverse events (e.g., nausea, gastrointestinal discomfort) will be monitored and recorded throughout the 3-month supplementation period to assess safety.

Sponsors and collaborators

Lead sponsor

Pico Entech Co., Ltd.

Industry

Collaborators

  • Korea University Anam Hospital

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 20, 2025
Registry last updated
Nov 20, 2025

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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