UBMD Neurology
Williamsville, New York, 14221, United States
NCT Number: NCT06339034
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.
This study is active but is not currently recruiting participants.
Notify Me40 year–80 year
All sexes
Interventional
Phase 1 / Phase 2
Williamsville, New York, 14221, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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 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.
5mg of elemental lithium/capsule
Cellulose-filled capsules
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).
Time frame: Change from baseline (BL) to 24 week
PBMC Nurr1 mRNA expression using Taqman PCR.
Time frame: Change from baseline (BL) to 24 week
Serum NfL assessed using SIMOA platform by Quanterix (Lexington, MA)
Time frame: Change from baseline (BL) to 24 week
PBMC SOD-1 mRNA expression using Taqman PCR
Time frame: Change from baseline (BL) to 24 week
Assessed using ELISA
Time frame: Change from baseline (BL) to 24 week
Assessed using ELISA
Time frame: Change from baseline (BL) to 24 week
Assessed using ELISA
Time frame: Change from baseline (BL) to 24 week
Serum GFAP assessed using SIMOA platform by Quanterix (Lexington, MA)
Time frame: Change from baseline (BL) to 24 week
Assessed in the "on" state. Score range 0-132 with higher scores indicating worse outcomes.
Time frame: Change from baseline (BL) to 24 week
Score range 0-30 with higher scores indicating better outcomes.
Time frame: Change from baseline (BL) to 24 week
Score range 0-48 with higher scores indicating worse outcomes.
Time frame: Change from baseline (BL) to 24 week
Score range 0-15 with higher scores indicating worse outcomes.
Time frame: Change from baseline (BL) to 24 week
Score range 9-63 with higher scores indicating worse outcomes.
Time frame: Change from baseline (BL) to 24 week
Score range 0-28 with higher scores indicating worse outcomes.
Time frame: Change from baseline (BL) to 24 week
Score range 0-32 with higher scores indicating worse outcomes.
Time frame: Change from baseline (BL) to 24 week
Higher scores indicate higher dose of dopaminergic therapy.
Time frame: Throughout 24 week study
Number of patients with any and serious adverse events and number who withdraw from the study.
State University of New York at Buffalo
Other
Repurposing Lithium as a Disease-modifying Therapy in Parkinson's Disease: A Randomized Controlled Trial
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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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