CompletedNot Applicable

Application of Auricular Point Sticking in Patients With Taste Alteration

China120 participantsStarted 2023-06-03

Plain-language summary

To explore the intervention effect of auricular point sticking on chemotherapy-induced taste alterations in cancer patients, and analyze its relationship with quality of life, nutritional status and psychology of patients.

Who can participate

Age range

18 Years – 85 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients with malignant tumors diagnosed by histopathology or pathology;
. Age ≥18 years old;
. Patients who received platinum-based chemotherapy and completed at least one cycle of chemotherapy;
. According to the chemotherapy-induced taste Changes Scale (CiTAS), the score of patients was ≥6;
. Patients voluntarily participated in the treatment with good compliance and adherence.

Exclusion criteria

. Patients with treatment plan adjustment or concurrent radiotherapy;
. Patients with abnormal taste and malnutrition caused by various reasons before chemotherapy;
. Patients with inflammation of the external ear or eczema, ulcers, chilblain in the pressing area;
. Allergic or intolerant to adhesive stickers;
. Those who were lost to follow-up or withdrew voluntarily;
. Patients enrolled in other studies at the same time.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Taste alterations

Timeframe: T1: Baseline. T2:2 weeks. T3: 4 weeks. T4:5 weeks.

Trial details

NCT IDNCT05868850

SponsorAffiliated Hospital of Jiangnan University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-09-30

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