Can heated herb plasters boost blood counts after chemotherapy?
NCT ID NCT07790692
First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time
Summary
This trial tests whether heated traditional Chinese medicine plasters can help cancer patients recover from chemotherapy-induced anemia and low blood cell counts. Participants apply the plaster to a specific point on the navel for one hour daily over two weeks. Researchers compare the heated plaster against a sham version to see if it improves blood counts, reduces the need for transfusions or growth factor injections, and enhances quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Heated traditional Chinese medicine plaster applied to the Shenque point, with moxibustion heat
- What this could lead to
- If it works, this could offer a non-drug way to ease chemotherapy-related blood cell drops, reduce transfusions, and improve quality of life for cancer patients.
- What could go wrong
- This is a small, early trial with 40 participants, so results may not apply broadly. The treatment is not a cure and may not improve blood counts or symptoms for everyone.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Feb 2026
- Lead sponsor
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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
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21 years and older
- Sex
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Anyone
- Healthy volunteers
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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: Patients were eligible if they were: (i) had a diagnosis of stage I-IV cancer. (ii) be aged 20 years or older. (iii)hematological dysfunction: have experienced a WBC count of \<4000/μL or ANC \<1500/μL after starting chemotherapy. (iv) can understand and voluntarily sign the informed consent form t Exclusion Criteria: The following conditions disqualify participants from the study: (i) Patients who are unsuitable for moxibustion, including those with wounds at the moxibustion site. (ii)Individuals who refuse to sign the informed consent form. (iii) Minors, pregnant women, individuals with mental illnesses, those at risk of harm, or vulnerable groups. (iv)Leukemia patients, as the disease itself affects blood cell changes. (v) Those who have used leukopoietic agents or received blood transfusions within the past month.
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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
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Taichung armed forces gereral hospital
Taichung, Taiping District, 411228, Taiwan
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