Pharmacokinetics Centella Asiatica Product (CAP) in Mild Cognitive Impairment

Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2019
PRIMARY OBJECTIVES: 1. To assess the bioavailability and rate of clearance of Centella asiatica derived compounds in mildly demented elders on cholinesterase inhibitor therapy through a pharmacokinetic study. 2. To determine the acute tolerability of a Centella asiatica product in mildly demented elders on cholinesterase inhibitor therapy. OUTLINE: Participants will orally consume a single administration of a standardized Centella asiatica water extract product (CAP). Two doses (2g and 4g CAW) will be administered on separate occasions, at least two weeks apart. The levels of known bioactive compounds present in Centella asiatica will be measured in human plasma and urine over 12 hours after administration of each of the doses.
Epistemonikos ID: 94f1bd3ccfd9556d661cdf0a7d7cbe7f200e1f42
First added on: May 22, 2024