Lingzhi (CP003) for chronic fatigue syndrome and post-COVID fatigue
Official title: A Randomized, Waitlist-controlled Clinical Study on the Efficacy and Safety of Lingzhi-containing Dietary Supplement CP003 on Chronic Fatigue and Post-COVID Fatigue
Run by The University of Hong Kong · NCT06739720 · Data updated 2026-11-12
This trial tests whether the Lingzhi supplement CP003 can help people with chronic fatigue syndrome or fatigue after COVID-19 and whether it is safe to take.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Ages | 40 Years to 60 Years |
| Sex | All |
| Enrollment | 130 (estimated) |
| Sponsor | The University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | January 2, 2025 |
| Main results expected | January 15, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | September 21, 2026 |
| Trial ID | NCT06739720 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults meeting Fukuda criteria for CFS/ME or with persistent fatigue after SARS-CoV-2 infection who can complete a 6-week treatment and online fatigue surveys.
✕Probably not a fit
Individuals with recent participation in herbal supplements, other significant medical conditions, acute inflammation, or pregnancy plans in the next 3 months may not benefit or participate safely.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, controlled study compares CP003 Lingzhi capsules to a waitlist control in adults with chronic fatigue syndrome or post-COVID fatigue. Participants take five capsules daily for six weeks and undergo two blood tests, plus fatigue and quality-of-life questionnaires. The study aims to determine if CP003 reduces fatigue symptoms and how it affects safety, immune markers, and inflammation. Results will inform whether CP003 could be a beneficial, safe option for these fatigue conditions. The lead institution is The University of Hong Kong, with collaboration from the Innovation and Technology Commission.
Why it matters
Potential benefit: If successful, CP003 could provide a new, accessible option to reduce fatigue and improve quality of life for patients with CFS/ME or post-COVID fatigue.
How similar studies have gone: Prior studies of Lingzhi-related interventions for fatigue are limited; this trial explores a novel application with a controlled design.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Meet the Fukuda diagnostic definition of CFS/ME or have persisting fatigue after the infection of SARS-CoV-2 * Are able to complete a 6-week course of intervention; * Able to complete the online validated fatigue surveys. Exclusion Criteria: * Have participated in any type of complements or herbal medicine within the past six months; * Have serious medical conditions that might limit their participation in this intervention; * Diagnosed with acute inflammation; * Are pregnant or are planning a pregnancy in the next 3 months.
Where it's running
-
Specialist Clinical Centre for Teaching and Research, School of Chinese Medicine, The University of Hong Kong
Hong Kong, Hong Kong Recruiting
Study contacts
- Study coordinator: Tung Leong Fong
- Email: tlfong@hku.hk
- Phone: +852 5660 4020
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.