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RecruitingMajor Depression

Leucine in Midlife Depression

Eligible age

35–65 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

The study aims to investigate the effects of a 6-week leucine challenge on brain chemistry, connectivity, and behavior in people with midlife depression. The researchers will compare the leucine and an active comparator arm (lysine) for 6 weeks.

Sponsor: Emory University

You may qualify if…

  • Able and willing to provide informed consent
  • Diagnosis of major depression per Structured Interview for DSM-V (SCID-V)
  • Moderate to severe depression- Inventory of Depressive Symptoms - Self Reported (IDS-SR score \>34).
  • SHAPS score \>30 on the 0-56 scale
  • Body mass index (BMI) between 20-35 kg/m2
  • Plasma CRP \>1 mg/L
  • No contraindications to MRI
  • Availability of friends or family for transportation after lumbar puncture procedure

You may not qualify if…

  • Leucine-Specific:
  • History of maple syrup urine disease
  • Risk of hypoglycemia (unstable diabetes)
  • History of vitamin B6 deficiency, relative
  • Lysine-Specific:
  • On calcium supplements, relative
  • History of renal/gall stones (could cleared by a primary care provider)
  • Cognitive:

Where it's recruiting

Georgia

Atlanta

Source: ClinicalTrials.gov · NCT06580145 · last updated 2025-04-24

Leucine in Midlife Depression · TrialPath