RCT of Efficacy and Safety of CP003 on CFS/ME or Post-COVID Fatigue
- NCT ID
- NCT06739720
- Registry status
- Not yet recruiting
- Study type
- Not specified in the registry data
- Phase
- Phase 2 / Phase 3
- Sponsor
- The University of Hong Kong
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 130 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility 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.
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Hong Kong
Sample of listed locations
- Specialist Clinical Centre for Teaching and Research, School of Chinese Medicine, The University of Hong Kong — Hong Kong, Hong Kong — Site recruitment status not specified in the registry data
Study details
- Start date
- January 2, 2025
- Primary completion date
- June 30, 2026
- First posted
- December 18, 2024
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT06739720
- Registry last updated
- December 18, 2024
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT06739720 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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