Clinical trial Recruiting at 1 site Phase2; Phase3 Interventional Ages 40 to 60

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

PhasePhase2; Phase3
Study typeInterventional
Ages40 Years to 60 Years
SexAll
Enrollment130 (estimated)
SponsorThe University of Hong Kong
Academic / other
Locations1 site (Hong Kong)
StatusRecruiting
StartedJanuary 2, 2025
Main results expectedJanuary 15, 2026
Study endsDecember 31, 2026
Registry record updatedSeptember 21, 2026
Trial IDNCT06739720 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.