Active, not recruitingPhase 2NCT06519357
A Single-center, Self-controlled, Prospective Case Series Pilot Study to Assess the Effect of Lamivudine (3TC) on Neurocognitive Impairment Biomarkers and Type-I IFN (Interferon)-Stimulated Genes in the Plasma of Patients With Mild Cognitive Impairment (MCI)
Studying Lymphangioleiomyomatosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
- Intervention
- Lamivudine 300 MG(drug)
- Enrollment
- 23 target
- Eligibility
- 55-90 years · All sexes
- Timeline
- 2024 – 2026
Study locations (1)
- Germans Trias I Pujol Hospital, Badalona, BARCELONA, Spain
Collaborators
IrsiCaixa
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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