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Acupoint Application for Chemotherapy-Induced Nausea and Vomiting in Lung Cancer

RecruitingNAAges 18 Years - 75 YearsAllXiu Huang
NCT07768124 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This single-center, randomized, controlled study evaluates whether acupoint application added to standard 5-HT3 receptor antagonist anti-nausea medication improves control of chemotherapy-induced nausea and vomiting in adults with lung cancer receiving first-line platinum-based chemotherapy. Participants will be randomly assigned to receive either acupoint application plus a 5-HT3 receptor antagonist or the 5-HT3 receptor antagonist alone for one chemotherapy cycle. The study will compare complete control of delayed nausea and vomiting between the two groups.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Pathologically or cytologically confirmed lung cancer. * Scheduled to receive first-line platinum-based chemotherapy. * Aged 18 to 75 years. * Karnofsky Performance Status (KPS) score ≥ 60. * Expected survival ≥ 3 months. * Voluntarily signed written informed consent. Exclusion Criteria: * Known allergy to any component of the acupoint plaster. * Severe skin disease, infection, or breakdown at the planned acupoint sites. --Pregnant or lactating women. * Cognitive impairment or psychiatric disorder that prevents completion of study assessments. * Participation in another interventional clinical trial within 30 days prior to enrollment.
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What it tests

  • 5-HT3 receptor antagonist (e.g., ondansetron)
  • Acupoint application
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Where

1 site
The Affiliated Yongchuan Hospital of Chongqing Medical University
Chongqing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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