75
Participants
Start Date
February 1, 2024
Primary Completion Date
December 1, 2024
Study Completion Date
April 30, 2025
Wild thyme extract
All patients will be randomized (1:1) to receive the active thyme extract (600 mg/capsule/day or 600 mg/capsule/day of microcrystalline cellulose) in the form of capsules, administered orally and daily for 2 months
Placebo
600 mg/day microcrystalline cellulose
Alba Rodriguez Nogales, Granada
Fundación Pública Andaluza para la Investigación Biomédica Andalucía Oriental
OTHER