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Ear acupressure: a new weapon against chemotherapy side effects?
NCT ID NCT07760766
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This trial tests whether adding auricular acupressure—using small seed patches on specific ear points—to standard antiemetic medication can better prevent nausea and vomiting in people receiving highly emetogenic chemotherapy. About 332 patients with solid tumors will be randomly assigned to receive either real acupressure or a sham version, alongside their usual antiemetic therapy. The main goal is to see if more patients achieve complete protection from delayed nausea and vomiting (24–120 hours after chemo) with the acupressure add-on.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Auricular acupressure using Vaccaria seed ear patches applied to specific ear points, added to standard triple antiemetic therapy
- What this could lead to
- If effective, this noninvasive technique could become a standard add-on to reduce delayed nausea and vomiting in chemotherapy patients, improving quality of life and treatment adherence.
- What could go wrong
- The trial is early-stage and may show no added benefit over sham. Results depend on patient adherence and may not generalize to all chemotherapy regimens.
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
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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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About 332 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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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18 to 75 years
- 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 * Age 18-75 years, either sex. * Malignant solid tumor confirmed by histopathology. ③ Chemotherapy-naïve, planned to receive a single-day intravenous highly emetogenic chemotherapy (HEC) regimen, including: * Cisplatin-containing regimens (dose ≥50 mg/m²); * Anthracycline plus cyclophosphamide (AC/EC) regimens; * Carboplatin AUC ≥4; * Other highly emetogenic chemotherapy regimens recognized by guidelines. ④ In accordance with guideline recommendations for HEC regimens, the triple regimen of NK-1 RA + 5-HT₃ RA + dexamethasone is used: ⑤ ECOG performance status score 0-1. ⑥ Life expectancy ≥ 6 months. ⑦ Voluntarily signed informed consent, and able to understand and complete the patient diary. Exclusion Criteria * Nausea or vomiting already present within 24 hours prior to enrollment. * Symptomatic brain metastases, gastrointestinal obstruction, or other organic diseases likely to cause nausea and vomiting. * Local skin breakdown, infection, or deformity of the auricle, or allergy to adhesive tape/Vaccaria seeds (Wang Bu Liu Xing). ④ Planned use of olanzapine, thalidomide, or other antiemetic agents not specified in the protocol as part of the routine prophylactic antiemetic regimen during this chemotherapy cycle (i.e., those receiving a quadruple regimen or other non-standard prophylactic regimens). ⑤ Long-term regular use (e.g., more than 3 times per week) of benzodiazepines, antipsychotics, or sedative-hypnotics; or known history of drug abuse/dependence. ⑥ Severe mental illness or cognitive impairment that precludes cooperation with assessments. ⑦ Receipt of ear acupuncture or auricular acupressure (ear seeds) within 4 weeks prior to enrollment. ⑧ Pregnant or lactating women.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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The First Hospital of China Medical University
Shenyang, Liaoning, 110001, China
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