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NCT Number: NCT06339034

Repurposing Lithium for Parkinson's Disease: a RCT

This study will examine the effects of lithium 20mg/day compared to placebo on MRI and blood-based biomarkers among 20 early-stage Parkinson's disease patients.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

UBMD Neurology

Williamsville, New York, 14221, United States

About this study

In observational studies, small daily doses of lithium have been associated with a 77% reduced risk of developing Parkinson's disease (PD). In addition, lithium therapy has been effective in preventing neuronal death and behavioral symptoms in several PD animal models. Recently, our group has shown 24-weeks of low-dose lithium therapy in PD to improve both MRI and blood-based biomarkers implying that lithium may be slowing the progression of the disease. However, these findings stem from only three of four patients receiving MRIs. A larger study will be required to determine if these promising results can be replicated. The proposed study will enroll 20 additional PD patients who will be randomly assigned to receive either lithium 20mg/day or identically-appearing placebo capsules for 24 weeks. This will be a double-blind study meaning that neither the patients nor the study team will know to which therapy patients have been assigned. Positive results from this study will support further research on lithium that could eventually support lithium as a disease-modifying therapy for PD that could improve patients' long-term prognoses.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Have PD for <4 years diagnosed by a movement disorder specialist. Have normal thyroid and renal function at the screening visit. Have no previous exposure to lithium therapy. Have no history of brain surgery. Have no hx of brain imaging findings suggesting another neurological condition besides PD.

Have no use of tobacco or THC products for >1 year. Have stable PD medications for >30 days without current need for adjustments in the investigator's opinion.

Have stable psychiatric and diuretic medications for >60 days with no anticipated need for changes for at least 24 weeks.

Have no active medical or psychiatric condition that may interfere with study procedures in the investigator's opinion.

Exclusion criteria

  • Have PD for >4 years or does not have PD. Have abnormal normal thyroid and renal function at the screening visit. Have previous exposure to lithium therapy. Have history of brain surgery. Have hx of brain imaging findings suggesting another neurological condition besides PD.

Have use of tobacco or THC products within the past year. Have PD medication adjustments within 30 days or needs PD medication adjustments in the investigator's opinion.

Have psychiatric or diuretic medication adjustments within the last 60 days or is anticipated to need changes over next 24 weeks.

Have active medical or psychiatric condition that may interfere with study procedures in the investigator's opinion.

Treatment and study plan

Lithium

Dietary Supplement

5mg of elemental lithium/capsule

Placebo

Other

Cellulose-filled capsules

Primary outcomes

  1. MRI-derived free water (FW) levels.

    Time frame: Change from baseline (BL) to 24 week

    FW in the posterior substantia nigra (pSN), dorsomedial nucleus of the thalamus (DMN-T) and the nucleus basalts of Meynert (nbM).

  2. Peripheral blood mononuclear cell (PBMC) nuclear receptor-related 1 protein (Nurr1) mRNA expression

    Time frame: Change from baseline (BL) to 24 week

    PBMC Nurr1 mRNA expression using Taqman PCR.

  3. Serum neurofilament light chain (NfL)

    Time frame: Change from baseline (BL) to 24 week

    Serum NfL assessed using SIMOA platform by Quanterix (Lexington, MA)

Secondary outcomes

  1. PBMC superoxide dismutase type-1 (SOD-1) mRNA expression

    Time frame: Change from baseline (BL) to 24 week

    PBMC SOD-1 mRNA expression using Taqman PCR

  2. PBMC pS9/total glycogen synthase kinase-3B (GSK-3B) ratio

    Time frame: Change from baseline (BL) to 24 week

    Assessed using ELISA

  3. PBMC pThr308 and pS473/total protein kinase B (Akt) ratios

    Time frame: Change from baseline (BL) to 24 week

    Assessed using ELISA

  4. Serum interleukin-6

    Time frame: Change from baseline (BL) to 24 week

    Assessed using ELISA

  5. Serum glial fibrillary acidic protein (GFAP)

    Time frame: Change from baseline (BL) to 24 week

    Serum GFAP assessed using SIMOA platform by Quanterix (Lexington, MA)

  6. Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III (Motor Examination)

    Time frame: Change from baseline (BL) to 24 week

    Assessed in the "on" state. Score range 0-132 with higher scores indicating worse outcomes.

  7. Montreal Cognitive Assessment (MoCA)

    Time frame: Change from baseline (BL) to 24 week

    Score range 0-30 with higher scores indicating better outcomes.

  8. Parkinson's Anxiety Scale

    Time frame: Change from baseline (BL) to 24 week

    Score range 0-48 with higher scores indicating worse outcomes.

  9. Geriatric Depression Scale-15

    Time frame: Change from baseline (BL) to 24 week

    Score range 0-15 with higher scores indicating worse outcomes.

  10. Fatigue Severity Scale

    Time frame: Change from baseline (BL) to 24 week

    Score range 9-63 with higher scores indicating worse outcomes.

  11. Insomnia Severity Index

    Time frame: Change from baseline (BL) to 24 week

    Score range 0-28 with higher scores indicating worse outcomes.

  12. Parkinson's Disease Questionnaire-8

    Time frame: Change from baseline (BL) to 24 week

    Score range 0-32 with higher scores indicating worse outcomes.

  13. Levodopa equivalent daily dose (LEDD)

    Time frame: Change from baseline (BL) to 24 week

    Higher scores indicate higher dose of dopaminergic therapy.

Other outcomes

  1. Adverse events

    Time frame: Throughout 24 week study

    Number of patients with any and serious adverse events and number who withdraw from the study.

Sponsors and collaborators

Lead sponsor

State University of New York at Buffalo

Other

Collaborators

  • Cure Parkinson's

Registry information

Official study title

Repurposing Lithium as a Disease-modifying Therapy in Parkinson's Disease: A Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Apr 1, 2024
Registry last updated
Jun 16, 2026

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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