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Recruiting NCT05762250

NCT05762250 Auricular Acupuncture in Patients With Advanced Cancer: a Randomized Clinical Trial.

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Clinical Trial Summary
NCT ID NCT05762250
Status Recruiting
Phase
Sponsor University Hospital Tuebingen
Condition Fatigue
Study Type INTERVENTIONAL
Enrollment 125 participants
Start Date 2023-08-13
Primary Completion 2026-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Auricular Acupuncture

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 125 participants in total. It began in 2023-08-13 with a primary completion date of 2026-06.

⚠ 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

In the present study, the effect of ear acupressure treatment according to the NADA protocol on the quality of life of patients with advanced tumour diseases. (all stages) will be investigated. Furthermore, the effect of ear acupressure on anxiety and depression, pain, fatigue and sleep of the patients will be assessed.

Eligibility Criteria

Inclusion Criteria: * Adult patients with advanced tumour diseases on current therapy, who suffer from persistent disease- or therapy-associated symptoms and limitations (screening by distress thermometer, score ≥ 5) * Informed consent. Exclusion Criteria: * medical reasons or * a mental condition which, in the opinion of the investigator, does not allow the patient to participate in the study, * a planned radiation therapy in the area of the skull (to avoid potential scattered radiation), * a missing legally binding signature on the informed consent form, * participation in another acupuncture/acupressure study.

Contact & Investigator

Central Contact

Claudia Loeffler, Dr

✉ loeffler_C@ukw.de

📞 +49 93120144966

Principal Investigator

Claudia Loeffler, Dr

PRINCIPAL INVESTIGATOR

Wuerzburg University Hospital

Frequently Asked Questions

Who can join the NCT05762250 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Fatigue. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05762250 currently recruiting?

Yes, NCT05762250 is actively recruiting participants. Contact the research team at loeffler_C@ukw.de for enrollment information.

Where is the NCT05762250 trial being conducted?

This trial is being conducted at Stuttgart, Germany, Würzburg, Germany.

Who is sponsoring the NCT05762250 clinical trial?

NCT05762250 is sponsored by University Hospital Tuebingen. The principal investigator is Claudia Loeffler, Dr at Wuerzburg University Hospital. The trial plans to enroll 125 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology