Clinical Trial

RCT of Efficacy and Safety of CP003 on CFS/ME or Post-COVID Fatigue

Not Yet Recruiting Phase 2/3
View on ClinicalTrials.gov →
Record status
This record was last updated December 18, 2024 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
The goal of this clinical trial is to test if a Lingzhi supplement (CP003) helps people with chronic fatigue or post-COVID fatigue feel better. It will also check if the supplement is safe to use. The main questions it aims to answer are: Does the Lingzhi supplement reduce fatigue symptoms? Is it safe to take? How does it affect the body's immune system and inflammation? Researchers will compare people taking the Lingzhi supplement to those who don't take anything (waitlist group) to see if it works. Participants will: * Take 5 capsules once daily for 6 weeks (or wait to start treatment if in waitlist group) * Visit the clinic 2 times for blood tests (before and after taking the supplement) * Complete questionnaires 3 times about their fatigue and quality of life (4 times questionnaires for waitlist group)
Trial Details
NCT Number NCT06739720
Lead Sponsor The University of Hong Kong
Collaborators: Innovation and Technology Commission, Hong Kong
Conditions Chronic Fatigue Syndrome (CFS), Post-COVID ME/CFS
Enrollment 130 participants
Start Date 2025-01-02
Primary Completion 2026-06-30 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2024-12-18