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Recruiting NCT02304913

NCT02304913 Hypoglossal Acupuncture for Dysgeusia in Patients Undergoing Chemotherapy

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Clinical Trial Summary
NCT ID NCT02304913
Status Recruiting
Phase
Sponsor Universität Duisburg-Essen
Condition Acupuncture
Study Type INTERVENTIONAL
Enrollment 75 participants
Start Date 2015-01-01
Primary Completion 2027-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Hypoglossal acupunctureSham acupunctureDietary recommendations

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 75 participants in total. It began in 2015-01-01 with a primary completion date of 2027-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled trial aims to investigate hypoglossal acupuncture in comparison to sham acupuncture and standard medical treatment (dietary recommendations) in the treatment of dysgeusia in cancer patients undergoing chemotherapy.

Eligibility Criteria

Inclusion Criteria: * Initial treatment with platinum-containing or taxane-based CTX (regardless of the the length of the CTX cycle) * Senological, gynecological or internistic tumors * Phantogeusia (on average ≥4 NRS) * Willingness to participate in the study and written informed consent Exclusion Criteria: * Severe stomatitis * Dysgeusia before the CTX based on neurological diseases, diabetes, or the ingestion of drugs with taste disorders as side effects * Leucopenia/neutropenia * Intake of anticoagulants * Smoking * Severe physical or mental comorbidity (due to which the patient is unable to participate in the study) * Participation in other CAM treatments within the integrative oncology care * Participation in other studies on the effectiveness of interventions for oral complications

Contact & Investigator

Central Contact

Heidemarie Haller, PhD

✉ heidemarie.haller@uk-essen.de

📞 +4920172377382

Principal Investigator

Gustav Dobos, Prof., MD

STUDY DIRECTOR

Center for Integrative Medicine and Health, University Hospital Essen, University of Duisburg-Essen

Frequently Asked Questions

Who can join the NCT02304913 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Acupuncture. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT02304913 currently recruiting?

Yes, NCT02304913 is actively recruiting participants. Contact the research team at heidemarie.haller@uk-essen.de for enrollment information.

Where is the NCT02304913 trial being conducted?

This trial is being conducted at Essen, Germany, Mannheim, Germany, Stuttgart, Germany.

Who is sponsoring the NCT02304913 clinical trial?

NCT02304913 is sponsored by Universität Duisburg-Essen. The principal investigator is Gustav Dobos, Prof., MD at Center for Integrative Medicine and Health, University Hospital Essen, University of Duisburg-Essen. The trial plans to enroll 75 participants.

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