Ancient herbs take on long COVID: a trial tests whether chinese medicine can soothe persistent fatigue
NCT ID NCT04924881
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This phase 2 trial tests whether a Chinese herbal formula, COVID Rehab Formula, can reduce fatigue and other lingering symptoms in people who have recovered from COVID-19. Participants take the herbal granules or a placebo daily for 8 weeks. The study focuses on those with ongoing fatigue plus at least one other symptom, such as breathlessness, cough, or sleep problems.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a Chinese herbal formula called COVID Rehab Formula granules
- What this could lead to
- If it works, this could offer a treatment option for persistent fatigue and other lingering symptoms after COVID-19.
- What could go wrong
- This is a small, early-phase trial with only 68 participants, so results may not apply widely. Herbal formulas can also have side effects or interact with other medications.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
68 people
The number who actually took part.
- Started
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Jul 2021
- Finished
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Oct 2022
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged above 18; * Have fatigue and one more residue symptoms (e.g. dyspnoea, sleep disturbance, cough, loose stool, abdominal distension, loss of appetite, dizziness, etc.) at least 5 weeks after discharge * Patients are diagnosed with "lung-spleen qi deficiency"(肺脾氣虛) and/or"dual deficiency of qi and yin"(氣陰兩虛) by a Chinese Medicine Practitioner * Voluntary written consent. Exclusion Criteria: * Still being SARS-CoV-2 positive * Known severe medical conditions, such as cardiovascular, liver or renal dysfunction, diabetes mellitus, cancers, cerebrovascular diseases, blood system diseases; * Impaired hematological profile and liver / renal function; * No concomitant non-steroidal anti-inflammatory drugs (NSAIDs), steroids, antibiotics, prebiotics, probiotics within 4 weeks; * Known allergic history to any Chinese herbal medicines; * Known pregnancy or lactating.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The Chinese University of Hong Kong
Shatin, Hong Kong
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