Green tea mist tested against COVID lung inflammation in cancer patients
NCT ID NCT06924749
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed Phase 2 trial tested whether inhaling a green tea extract called EGCG could help cancer patients with moderate-to-severe COVID-19 pneumonia. 111 participants received either EGCG mist or a placebo three times daily for 7 days. The study looked at lung CT scan improvements, symptom relief, and safety. EGCG is known for anti-inflammatory and antiviral effects, but results are not yet available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- EGCG (epigallocatechin-3-gallate), a green tea extract, given as an inhaled mist
- What this could lead to
- If it works, this could offer a safe, plant-based treatment option for COVID-19 pneumonia in cancer patients, reducing lung inflammation and improving recovery.
- What could go wrong
- This is a small, completed Phase 2 trial with no published results yet. The benefit may be modest or not better than standard care, and the findings may not apply to non-cancer patients.
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
-
111 people
The number who actually took part.
- Started
-
Jun 2023
- Finished
-
Jul 2024
- 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
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosed malignant tumors by pathology or cytology * COVID-19 with a confirmed positive polymerase chain reaction or antigen test result for SARS-CoV-23 * moderate-to-severe COVID-19 pneumonia (defined as any radiographic evidence of pulmonary infiltrates and oxygen saturation \>94% on room air) * Pulmonary function of the patient can be treated with aerosol inhalation for 7 days Exclusion Criteria: * Current or recent progresses rapidly and may develop into a Critical illness with coronavirus in a short period of time * Caused by other viruses such as cytomegalovirus, as well as pneumocystis pneumonia, pulmonary edema, aspiration pneumonia and acute interstitial pneumonia * Any condition including medical, emotional, psychiatric, or logistical that, in the opinion of the Investigator would preclude the participant from adhering to the protocol or would increase the risk associated with study participation * known allergy or hypersensitivity to EGCG
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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
-
Hanxi Zhao
Jinan, Shandong, Shandong Cancer Hospital, China
-
Shan Dong cancer hospital and institute
Jinan, Shandong, 250117, China
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